Skip to main content
Download PDF

Neuroendocrine and squamous cell phenotypes of NUT carcinoma are potential diagnostic pitfalls that discriminating it from mimickers, such as small cell and squamous cell carcinoma

Diagnostic Pathology volume 19, Article number: 27 (2024) Cite this article

Abstract

Introduction

NUT carcinoma is a rare cancer associated with a poor prognosis. Because of its rarity, its diagnosis is challenging and is usually made by excluding other diagnoses. Immunohistochemical analysis is a reliable technique that contributes to a correct diagnosis, but overestimating the expression of neuroendocrine (NE) markers may result in an incorrect diagnosis. In this study, we established the immunohistochemical phenotypes of NUT carcinoma compared with tumors that mimic its phenotype to identify potential diagnostic pitfalls.

Methods

Eight cases of NUT carcinoma were examined along with eight basaloid squamous cell carcinomas and thirteen cases of small cell carcinoma using an immunohistochemical panel consisting of various antibodies.

Results

Of the eight NUT carcinomas, three patients had a smoking history. All the cases examined for INSM1 were positive (6/6, 100%), although the staining was somewhat weak. Among the NE markers, synaptophysin was variably positive in two NUT carcinomas (2/6, 33%); however, all cases were negative for ASCL1, chromogranin A, and CD56. Moreover, the squamous cell markers, p40 and CK5/6, were weakly expressed in 4/6 (67%) and 3/6 (50%) of the NUT carcinomas, respectively.

Conclusions

For tumors with an ambiguous morphology, applying the neuroendocrine phenotype of NUT carcinoma may be misleading; particularly, when distinguishing it from small-cell carcinoma. Similarly, null or weak expression of squamous cell markers may be observed in NUT carcinoma, but this differs from squamous cell carcinoma, which consistently demonstrates strong positivity for squamous cell markers.

Introduction

NUT carcinoma is a highly aggressive, poorly differentiated tumor hallmarked by a NUT gene rearrangement. Fusion partners include the bromodomain family members, BRD3 and BRD4 [1], or the methyltransferase NSD3 [2]. Most tumors occur in the thoracic, head, and neck regions [3, 4]. Pathologically, NUT carcinoma typically appears as sheets and nests of small- or intermediate-sized undifferentiated cells exhibiting a monomorphic appearance [1, 5], and occasionally contains a squamous cell component. A primitive morphological appearance can complicate the recognition as NUT carcinoma, particularly if there is a lack of characteristic squamous differentiation, such as abrupt keratinization. Immunohistochemical studies have facilitated rapid diagnosis by enabling the detection of NUT protein overexpression; however, because of its rarity and ambiguous protein expression, the correct diagnosis of NUT carcinoma is usually achieved by exclusion, which may lead to pitfalls during diagnosis.

Overestimating specific immunohistochemical expression may complicate the diagnostic process. For example, some NUT carcinomas express neuroendocrine markers, which may result in the misdiagnosis of neuroendocrine carcinoma if stained prior to performing NUT immunohistochemistry.

In the present study, we clarified the challenges of correctly diagnosing NUT carcinoma using immunohistochemistry and comparing the resulting profiles of NUT carcinoma with those of its mimickers, which are encountered in thoracic pathology, particularly basaloid squamous cell carcinoma (BSCC) and small cell lung carcinoma (SCLC).

Materials and methods

Case selection

The pathological database of the Cancer Institute Hospital of the Japanese Foundation for Cancer Research (JFCR), Tokyo, was reviewed. Tumors were selected from patients that were diagnosed or treated at the hospital between September 2015 and August 2020. Thoracic and nonthoracic NUT carcinomas, such as tumors originating in the ethmoid sinus, were included because of their high morphological similarity, irrespective of origin. BSCC and SCLC were randomly collected for comparison. The institutional review board approved the study at the JFCR (#2012–1042). The requirement for informed consent was waived and the study was performed following the principles of the Declaration of Helsinki.

Immunohistochemical staining and method of intensity scoring

Using formalin-fixed, paraffin-embedded tissues, 4-μm-thick slices were cut, stained with antibodies, and analyzed. Insulinoma-associated protein 1 (INSM1) [6, 7], achaete-scute complex-like 1 (ASCL1, MASH1) [8], chromogranin A, synaptophysin, and CD56 were used as conventional neuroendocrine markers, whereas p40 and CK5/6 were used as squamous cell markers. The proto-oncogene bcl-2 (BCL2) was included, which has a significant role in apoptosis inhibition and is highly expressed in SCLC [9, 10].

The following antibodies were used: NUT (rabbit monoclonal, C52B1, dilution 1:50, Cell Signaling, MA, US), chromogranin A (mouse monoclonal, clone DAK-A3, 1:2000; Dako, Carpinteria, CA, US), synaptophysin (mouse monoclonal, clone 27G12, 1:100; Leica Biosystems Newcastle Ltd, UK), CD56 (mouse monoclonal, clone 1B6, 1:50; Leica), INSM1 (mouse monoclonal, clone A-8, diluted 1:500; Santa Cruz, Dallas, TX, US), ASCL1 (mouse monoclonal, clone 24B72D11.1 (anti-MASH1), 1:50; BD Bioscience, Erembodegem, Belgium), p40 (mouse monoclonal, clone BC28, 1:200, Abcam, Cambridge, UK), CK5/6 (mouse monoclonal, clone D5/16B4, 1:200, Millipore, MA, US), TTF-1 (mouse monoclonal, clone 8G7G3/1, 1:100, Dako, Glostrup, Denmark), BCL2 (mouse monoclonal, 124, 1:200, Dako), ProGRP (monoclonal, clone PGCY-9, 1:10000, Fujirebio, Tokyo, Japan), and Ki-67 (mouse monoclonal, clone MIB-1, 1:200, Dako) (Table 1). Immunohistochemistry was carried out using a Bond-III automated immunostainer (Leica Biosystems Melbourne, Melbourne, Australia) and the Bond Polymer Refine Detection Kit as appropriate.

Table 1 Details of the antibodies used for immunohistochemistry
Full size table

The staining results for each antibody were interpreted using an H-score (HS), which was defined by the following equation: Σ (intensity) × (proportion, %). The intensity represents the relative level of tumor cell staining (0, 1, 2, or 3) and the proportion is the percentage of stained tumor cells with an intensity ranging from 0 to 100%. HS varied from 0 to 300. The expression of each antibody in the tumor cells was defined as strongly positive for HS ≥ 100, weakly positive (w +) when HS was ≥ 5, and negative when HS was < 5. For cases in which unstained slides were not available for assessment, 0–10% of stained cells were considered negative and more than 10% were positive.

Split fluorescence in situ hybridization (FISH) for NUT

Chromosomal translocation of the NUT locus was evaluated using FISH. Dual-color split FISH assays were performed on unstained slides (4-μm thick) using NUT DNA probes derived from bacterial artificial chromosome (BAC) clones. BAC clones were isolated and used as FISH probes. The names of the BAC clones are available upon request.

Fusion FISH to detect BRD4-NUT

Formalin-fixed, paraffin-embedded tumor sections underwent deparaffinization, rehydration, and pretreatment. Dual-color FISH probes targeted BRD4 and NUT loci. Post-hybridization, slides were washed and counterstained with DAPI. Fusion BRD4-NUT signals were identified as colocalized red and green signals under a fluorescence microscope. Fusion FISH analysis wad performed in case 4 and 8.

Next generation sequencing to confirm BRD4-NUT fusion

Genomic DNA was extracted from tumor samples and sequenced using Illumina HiSeq X. Libraries were prepared following TruSeq RNA Access Library Prep kit protocols. Sequencing aimed for a minimum 100 × depth. BRD4-NUT fusion detection was conducted using FusionCatcher [11].

Statistical analysis

To analyze statistical significance, a Student’s t-test, χ2 test, and Fisher’s exact test were used as considered appropriate to evaluate associations among the clinicopathological characteristics. The Kaplan–Meier method was used to estimate survival and the generalized Wilcoxon test was used to determine survival differences. All statistical analyses were done using EZR version 1.40 (Jichi Medical University Saitama Medical Center, Saitama, Japan) and statistical significance was defined as P < 0.05.

Results

Patient background

Patient details, including age, sex, smoking status, and prognosis, are listed in Table 2. Age at the time of diagnosis was significantly lower in the NUT carcinoma cases (44.5 ± 18.1 years) compared with that in the BSCC and SCLC cases (71.1 ± 9.9 years, p = 0.004, 67.8 ± 9.3 years, p = 0.007, respectively). Two of the eight NUT carcinoma cases and one case each of BSCC and SCLC were women. Five patients with NUT carcinoma were nonsmokers (5/8, 62.5%); however, all BSCC and SCLC cases were former or current smokers (0/21, nonsmokers 0%, Table 2), which was statistically significant (p = 0.0017). The NUT carcinoma specimens were obtained by transbronchial, needle, or excisional biopsies. As with BSCC and SCLC, six and two surgical resection specimens were used for comparison, respectively.

Table 2 Clinicopathological background of NUT carcinoma, basaloid squamous cell carcinoma, and small cell carcinoma
Full size table

Histological comparison of NUT carcinoma, BSCC, and SCLC

NUT carcinoma, BSCC, and SCLC exhibited a slightly similar morphology, in which they were composed of monomorphic tumor cells proliferating in a solid or sheet-like structure (Figs. 1, 2 and 3). Initially, only one case was correctly diagnosed as NUT carcinoma, whereas three were diagnosed as squamous cell carcinoma and two were considered SCLC, one with malignant cells and one a non-epithelial tumor. Of the eight NUT carcinoma cases, abrupt keratinization was observed in only three (3/8 and Cases 5, 6, and 8, Table 3).

Fig. 1
figure 1

Histological findings from hematoxylin & eosin staining and immunohistochemistry (NUT and INSM1) of NUT carcinoma. Positive nuclear staining of INSM1 was readily detected in tumor cells, although the staining intensity was generally weak

Full size image
Fig. 2
figure 2

Representative histology and immunohistochemistry of small cell lung carcinoma. Hematoxylin & eosin (a), NUT (b), chromogranin A showing cytoplasmic positivity in tumor cells (c). Both INSM1 (d) and ASCL1 (e) were positive in the nuclei

Full size image
Fig. 3
figure 3

Representative histology and immunohistochemistry of basaloid squamous cell carcinoma. Hematoxylin & eosin (a), NUT (b), synaptophysin (c), P40 was positive for tumor cells in the basal layer (d) and CK5/6 (e) strong and diffuse staining in the cytoplasm

Full size image
Table 3 Immunohistochemical profiles of NUT carcinoma, basaloid squamous cell carcinoma, and small cell carcinoma
Full size table

Results of immunohistochemistry with NUT

All NUT carcinomas were positive for NUT as determined by immunohistochemistry (Tables 3, 4 and Fig. 1), whereas none of the BSCC and SCLC were positive.

Table 4 Expression levels of each antibody evaluated using H-scores
Full size table

Results of the three conventional neuroendocrine markers as well as INSM1 and ASCL1

Synaptophysin was positive by immunohistochemical analysis for some NUT carcinoma cases; however, no cases were positive for chromogranin A or CD56. INSM1 is a promising marker for SCLC [6] and it was positive in all six NUT carcinoma cases available for staining as determined by immunohistochemistry (Fig. 1). Although the positive staining ratio was high, the intensity was weak (1 +) in contrast to the strong expression observed in SCLC (Table 3). ASCL1, which is also considered a useful marker for pulmonary small cell carcinoma, was negative in the NUT carcinomas.

Results of immunohistochemistry for TTF-1, p40, and CK5/6

All of the NUT carcinomas were negative for TTF-1 (0%,) whereas five were weakly or diffusely positive for p40. Two cases with abrupt keratinization exhibited strong positivity for one or both squamous cell markers; however, all BSCC cases, excluding one, were strongly positive for both p40 and CK5/6 (Tables 3 and 4).

Results of immunohistochemistry with BCL2 and ProGRP

The BCL2 oncoprotein has a unique role in the inhibition of programmed cell death (apoptosis), which results in tumorigenesis and chemoresistance. Immunohistochemical analysis of BCL2 revealed that it was upregulated in most small cell carcinomas [9]. All cases of BSCC and SCLC except one exhibited strong positive staining for BCL2. Interestingly, only two cases of NUT carcinoma were positive. ProGRP is a serum biomarker of small cell carcinoma and its protein expression was reported to be higher in SCLC tissues compared with control tissues [12]. ProGRP positivity was only observed in SCLC cases (7/13 = 54%) (Tables 3 and 4).

Results of Split FISH Analysis on NUT and BRD4-NUT Fusion Detection

Six NUT carcinoma that have FISH testing results all showed NUT translocation based on a split FISH analysis, as represented by isolated green and red signals flanking the NUT gene (Fig. 4). In Cases 4 and 8 BRD4-NUT fusion was confirmed by characterized by the co-localization of BRD4 and NUT-specific fluorescent signals.

Fig. 4
figure 4

The presence of two pairs of fused green and red signals was considered a normal finding (red arrow). In contrast, one fused red/green signal and one separate red and green signal are evident in the translocation-positive nuclei (yellow arrow)

Full size image

Next generation sequencing to detect BRD4-NUT fusion

HiSeq X sequencing technology coupled with FusionCatcher software identified the presence of the BRD4-NUTM1 fusion gene in case 8. The resulting sequence analysis revealed the following fusion junction:GGAGAGCTCCAGTGAGTCCAGCTCCTCTGACAGCGAAGACTCCGAAACA*GTGACCGCTCCAAAATTTCCAAGGACGTTTATGAGAACTTCCGTCAGTGG. Notably, the fusion was found to be out-of-frame, indicating a potential disruption in the normal reading frame of the genes involved.

Comparison of cancer-specific survival for NUT carcinoma, SCLC, and BSCC

Figure 5 shows the overall survival curves for the three groups. Four NUT carcinoma patients died within 5 months after diagnosis and early prognosis was considerably poor compared with that of the other two tumor types. However, the other four NUT carcinoma patients exhibited exceptional long-term survival; thus, there may be a subgroup of NUT carcinomas which have a good prognosis. Therefore, the statistical differences between NUT carcinoma and the other two diseases were insignificant (generalized Wilcoxon test: NUT vs. SCLC, p = 0.79; NUT vs. BSCC, p = 0.19; BSCC vs. SCLC, p = 0.0032).

Fig. 5
figure 5

Cancer-specific survival curves of NUT carcinoma, basaloid squamous cell carcinoma, and small cell carcinoma. The 1-year prognosis of NUT carcinoma was remarkably poor, although there may exist a subgroup of NUT carcinomas which have a better prognosis. The difference in long-term prognosis between BSCC or SCLC was statistically significant (p = 0.0032)

Full size image

Discussion

NUT carcinomas primarily exhibit an undifferentiated appearance both morphologically and immunohistochemically. The differential diagnosis of NUT carcinoma includes a wide variety of diseases, which may occasionally lead to an incorrect diagnosis. Immunohistochemistry is a reliable diagnostic tool for this tumor type, even when applied to small biopsy specimens; however, ambiguous immunohistochemical expression in NUT carcinomas can result in an incorrect diagnosis. Occasionally, NUT carcinomas present as a characteristic squamous-differentiated morphology, namely abrupt keratinization and some are defined as a subtype of squamous cell carcinoma [13], although squamous histology is not always apparent. Moreover, there is limited data with respect to neuroendocrine and squamous differentiation marker expression in NUT carcinomas and the results of previous studies have been inconclusive. Therefore, in the present study, we carried out a comprehensive immunohistochemical analysis of NUT carcinoma under similar conditions to identify the diagnostic pitfalls.

Several studies have been done on the immunohistochemical expression of NUT carcinomas (Table 5) [13,14,15,16,17]; however, the antibodies used varied depending on the site of origin and the possible differential diagnoses were diverse. In the present study, we focused on antibodies that can discriminate the major mimickers of thoracic origin, which include SCLC and BSCC. Therefore, the analysis of neuroendocrine and squamous cell markers is important. Sholl et al. [15] reported two cases of NUT carcinomas out of nine that were positive for synaptophysin and CD56, respectively, in the largest series of cases examined at a single institution, although the percentage (2/9 = 22%) was not high. Moreover, a recent study described a case of NUT carcinoma exhibiting positive synaptophysin expression that was misdiagnosed as a large cell neuroendocrine carcinoma [18]. These results suggest that placing a high priority on a specific antibody can lead to an incorrect diagnosis. Abrupt keratinization is a well-known feature of NUT carcinoma, which may represent an aggressive subtype of squamous cell carcinoma [19]. Unexpectedly, the positive staining rates for both p40 and CK5/6 in NUT carcinomas were variable and relatively low in our panel. One patient with abrupt keratinization exhibited strong positivity for both markers. Although p63 has been reported to have a high rate of positivity (Table 4), it has low specificity [20].

Table 5 Summary of the immunohistochemical studies of NUT carcinoma in the literature
Full size table

Recent studies have indicated that INSM1 is a sensitive and specific marker for SCLC [6, 7, 21,22,23,24]. It may be useful when other traditional neuroendocrine markers are negative. Only a few studies have considered INSM1 expression in NUT carcinoma [22, 25]. In the present study, all NUT carcinoma cases were positive for INSM1, which is in contrast to the results (0/5) reported by Tsai et al. [22], even though the same antibody was used. We consider the possibility of variations in sample size, technical aspects and biological variability among tumors, which could inherently cause differences in antigen expression. In the present study, it must be emphasized that the ratio of positive cells was relatively high (HS: 40–75%), although the staining intensity was weak (Table 4 and Fig. 1). Thus, positive INSM1 expression with an ambiguous morphology in small specimens may be a deceptive phenotype that requires careful consideration. Moreover, the expression of ASCL1, a transcription factor involved in the development of pulmonary neuroendocrine cells [6, 26], was not detected in NUT carcinomas. This was in contrast to the observed simultaneous expression of INSM1 and ASCL1, which was prevalent in the SCLC cases (Table 3). Discrepancies between the two neuroendocrine markers may also be useful for avoiding diagnostic traps. Although BCL2 and ProGRP are potential markers for SCLC [9, 10, 27], their specificity and sensitivity were lower in NUT carcinomas compared with that in SCLC.

NUT carcinoma should be suspected in patients without a history of smoking or minimal smoking with advanced disease during their initial diagnosis [18]. Most patients with NUT carcinoma generally have a short life expectancy; however, differences between prognostic risk groups defined by clinical and molecular profiles are statistically significant. In other words, primaries outside of the thorax with non-BRD4-NUT fusions (such as BRD3-NUT or NSD3-NUT) are associated with the best prognosis. A possible explanation for the worse prognosis in thoracic primaries is that they are less accessible and often present at a more advanced stage, or they may have a different cell biology [28]. In the present study, overall survival curves showed that non-thoracic origin had a better prognosis, though the difference was not statistically significant (data not shown).

Prompt and accurate diagnoses of lung tumors are essential to develop optimal treatments. Because most mimickers are smoking-related carcinomas, such as SCLC and BSCC, because more than half of the NUT carcinoma cases in this study were nonsmokers, may be a clue to consider the possibility of NUT carcinoma. In Case 1, small cell carcinoma was initially diagnosed. However, the neoplasm was refractory to standard therapeutic interventions, and further evaluation demonstrated immunohistochemical positivity for the NUT immunohistochemistry. For Case 2, histopathological assessment failed to identify a definitive carcinoma subtype and its origin, yet a thorough immunohistochemical analysis indicated positive staining for NUT. In Case 3, although initially characterized as small cell carcinoma, the presence of marked neutrophilic infiltration, indicative of NUT carcinoma, necessitated additional immunohistochemical investigation. In Case 4, a never smoker, an extensive immunohistochemical workup was previously conducted, assessing epithelial, mesenchymal, neurogenic, and melanocytic markers; only cytokeratin returned positive results. The high nuclear-to-cytoplasmic (N/C) ratio suggested small cell carcinoma, yet the presence of prominent nucleoli rendered the morphology indeterminate. Cases 5, 6, and 8, all never-smokers, were originally classified as squamous cell carcinoma. However, the abrupt keratinization observed prompted the application of immunohistochemical staining, fluorescence in situ hybridization (FISH), and next-generation sequencing to verify NUT carcinoma. We propose a more systematic use of NUT-specific immunohistochemistry in cases where the diagnosis is uncertain, especially when dealing with poorly differentiated tumors that present with ambiguous morphology. We also emphasize the need for a high index of suspicion in atypical presentations, particularly in younger patients and those without a significant smoking history, as highlighted by our study's findings.

In conclusion, NUT carcinomas exhibit a characteristic immunophenotype when squamous cell and neuroendocrine differentiation markers were examined. Our results indicate that reliable squamous cell markers are expressed variably among NUT carcinoma cases. The positive ratio for INSM1 in NUT carcinoma was relatively high; however, the intensity was low without exception. These results are the basis for the difference with BSCC and SCLC, which are sometimes indistinguishable based on morphology alone. Our findings underscore the necessity of conducting an exhaustive immunohistochemical evaluation to distinguish NUT carcinoma in cases presenting with ambiguous morphology and atypical clinical features.

Availability of data and materials

The datasets generated and/or analyzed in the present study are not publicly available, but are available from the corresponding author upon reasonable request.

References

  1. French CA. NUT midline carcinoma. Cancer Genet Cytogenet. 2010;203:16–20. https://doi.org/10.1016/j.cancergencyto.2010.06.007.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Suzuki S, Kurabe N, Ohnishi I, Yasuda K, Aoshima Y, Naito M, Tanioka F, Sugimura H. NSD3-NUT-expressing midline carcinoma of the lung: first characterization of primary cancer tissue. Pathol Res Pract. 2015;211:404–8. https://doi.org/10.1016/j.prp.2014.10.013.

    Article  CAS  PubMed  Google Scholar 

  3. Bauer DE, Mitchell CM, Strait KM, Lathan CS, Stelow EB, Lüer SC, Muhammed S, Evans AG, Sholl LM, Rosai J, Giraldi E, Oakley RP, Rodriguez-Galindo C, London WB, Sallan SE, Bradner JE, French CA. Clinicopathologic features and long-term outcomes of NUT midline carcinoma. Clin Cancer Res. 2012;18:5773–9. https://doi.org/10.1158/1078-0432.CCR-12-1153.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Huang QW, He LJ, Zheng S, Liu T, Peng BN. An overview of molecular mechanism, clinicopathological factors, and treatment in NUT carcinoma. BioMed Res Int. 2019;2019:1018439. https://doi.org/10.1155/2019/1018439.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Travis WD, Brambilla E, Burke AP, Marx A, Nicholson AG. WHO classification of tumours of the lung, pleura. Thymus and Heart J Thoracic Oncol. 2015;10:1240–2.

    Article  Google Scholar 

  6. Sakakibara R, Kobayashi M, Takahashi N, Inamura K, Ninomiya H, Wakejima R, Kitazono S, Yanagitani N, Horiike A, Ichinose J, Matsuura Y, Nakao M, Mun M, Nishio M, Okumura S, Motoi N, Ito T, Miyazaki Y, Inase N, Ishikawa Y. Insulinoma-associated Protein 1 (INSM1) is a better marker for the diagnosis and prognosis estimation of small cell lung carcinoma than neuroendocrine phenotype markers such as chromogranin A, synaptophysin, and CD56. Am J Surg Pathol. 2020;44:757–64. https://doi.org/10.1097/PAS.0000000000001444.

    Article  PubMed  Google Scholar 

  7. Mukhopadhyay S, Dermawan JK, Lanigan CP, Farver CF. Insulinoma-associated protein 1 (INSM1) is a sensitive and highly specific marker of neuroendocrine differentiation in primary lung neoplasms: an immunohistochemical study of 345 cases, including 292 whole-tissue sections. Mod Pathol. 2019;32:100–9. https://doi.org/10.1038/s41379-018-0122-7.

    Article  CAS  PubMed  Google Scholar 

  8. Furuta M, Sakakibara-Konishi J, Kikuchi H, et al. Analysis of DLL3 and ASCL1 in surgically resected small cell lung cancer (HOT1702). Oncologist. 2019;24:e1172–9. https://doi.org/10.1634/theoncologist.2018-0676.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Kaiser U, Schilli M, Haag U, Neumann K, Kreipe H, Kogan E, Havemann K. Expression of bcl-2—protein in small cell lung cancer. Lung Cancer. 1996;15:31–40. https://doi.org/10.1016/0169-5002(96)00568-5.

    Article  CAS  PubMed  Google Scholar 

  10. Pezzella F, Turley H, Kuzu I, Tungekar MF, Dunnill MS, Pierce CB, Harris A, Gatter KC, Mason DY. bcl-2 protein in non-small-cell lung carcinoma. N Engl J Med. 1993;329:690–4. https://doi.org/10.1056/NEJM199309023291003.

    Article  CAS  PubMed  Google Scholar 

  11. D. Nicorici, M. Satalan, H. Edgren, S. Kangaspeska, A. Murumagi, O. Kallioniemi, S. Virtanen, O. Kilkku. FusionCatcher – a tool for finding somatic fusion genes in paired-end RNA-sequencing data. bioRxiv. 2014. https://doi.org/10.1101/011650.

  12. Gong Z, Lu R, Xie S, Jiang M, Liu K, Xiao R, Shen J, Wang Y, Guo L. Overexpression of pro-gastrin releasing peptide promotes the cell proliferation and progression in small cell lung cancer. Biochem Biophys Res Commun. 2016;479:312–8. https://doi.org/10.1016/j.bbrc.2016.09.066.

    Article  CAS  PubMed  Google Scholar 

  13. Mao N, Liao Z, Wu J, Liang K, Wang S, Qin S, Dou Y, Lin H, Dong X. Diagnosis of NUT carcinoma of lung origin by next-generation sequencing: case report and review of the literature. Cancer Biol Ther. 2019;20:150–6. https://doi.org/10.1080/15384047.2018.1523852.

    Article  CAS  PubMed  Google Scholar 

  14. Evans AG, French CA, Cameron MJ, Fletcher CD, Jackman DM, Lathan CS, Sholl LM. Pathologic characteristics of NUT midline carcinoma arising in the mediastinum. Am J Surg Pathol. 2012;36:1222–7. https://doi.org/10.1097/PAS.0b013e318258f03b.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Sholl LM, Nishino M, Pokharel S, Mino-Kenudson M, French CA, Janne PA, Lathan C. Primary pulmonary NUT midline carcinoma: clinical, radiographic, and pathologic characterizations. J Thorac Oncol. 2015;10:951–9. https://doi.org/10.1097/JTO.0000000000000545.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Agaimy A, Fonseca I, Martins C, Thway K, Barrette R, Harrington KJ, Hartmann A, French CA, Fisher C. NUT carcinoma of the salivary glands: clinicopathologic and molecular analysis of 3 cases and a survey of NUT expression in salivary gland carcinomas. Am J Surg Pathol. 2018;42:877–84. https://doi.org/10.1097/PAS.0000000000001046.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Albrecht T, Harms A, Roessler S, Goeppert B. NUT carcinoma in a nutshell: a diagnosis to be considered more frequently. Pathol Res Pract. 2019;215:152347. https://doi.org/10.1016/j.prp.2019.01.043.

    Article  CAS  PubMed  Google Scholar 

  18. Pezzuto F, Fortarezza F, Mammana M, Pasello G, Pelosi G, Rea F, Calabrese F. Immunohistochemical neuroendocrine marker expression in primary pulmonary NUT carcinoma: a diagnostic pitfall. Histopathology. 2020;77:508–10. https://doi.org/10.1111/his.14166.

    Article  PubMed  Google Scholar 

  19. French CA, Rahman S, Walsh EM, Kühnle S, Grayson AR, Lemieux ME, Grunfeld N, Rubin BP, Antonescu CR, Zhang S, Venkatramani R, Dal Cin P, Howley PM. NSD3-NUT fusion oncoprotein in NUT midline carcinoma: implications for a novel oncogenic mechanism. Cancer Discov. 2014;4:928–41. https://doi.org/10.1158/2159-8290.CD-14-0014.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Bishop JA, Teruya-Feldstein J, Westra WH, Pelosi G, Travis WD, Rekhtman N. p40 (ΔNp63) is superior to p63 for the diagnosis of pulmonary squamous cell carcinoma. Mod Pathol. 2012;25:405–15. https://doi.org/10.1038/modpathol.2011.173.

    Article  CAS  PubMed  Google Scholar 

  21. Kriegsmann K, Zgorzelski C, Kazdal D, Cremer M, Muley T, Winter H, Longuespée R, Kriegsmann J, Warth A, Kriegsmann M. Insulinoma-associated Protein 1 (INSM1) in thoracic tumors is less sensitive but more specific compared with synaptophysin, chromogranin A, and CD56. Appl Immunohistochem Mol Morphol. 2020;28:237–42. https://doi.org/10.1097/PAI.0000000000000715.

    Article  CAS  PubMed  Google Scholar 

  22. Tsai HK, Hornick JL, Vivero M. INSM1 expression in a subset of thoracic malignancies and small round cell tumors: rare potential pitfalls for small cell carcinoma. Mod Pathol. 2020;33:1571–80. https://doi.org/10.1038/s41379-020-0517-0.

    Article  CAS  PubMed  Google Scholar 

  23. Rosenbaum JN, Guo Z, Baus RM, Werner H, Rehrauer WM, Lloyd RV. INSM1: A novel immunohistochemical and molecular marker for neuroendocrine and neuroepithelial neoplasms. Am J Clin Pathol. 2015;144:579–91. https://doi.org/10.1309/AJCPGZWXXBSNL4VD.

    Article  CAS  PubMed  Google Scholar 

  24. Fujino K, Yasufuku K, Kudoh S, et al. INSM1 is the best marker for the diagnosis of neuroendocrine tumors: comparison with CGA, SYP and CD56. Int J Clin Exp Pathol. 2017;10:5393–405.

    CAS  Google Scholar 

  25. Hung YP, Chen AL, Taylor MS, Huynh TG, Kem M, Selig MK, Nielsen GP, Lennerz JK, Azzoli CG, Dagogo-Jack I, Kradin RL, Mino-Kenudson M. Thoracic nuclear protein in testis (NUT) carcinoma: expanded pathological spectrum with expression of thyroid transcription factor-1 and neuroendocrine markers. Histopathology. 2021;78:896–904. https://doi.org/10.1111/his.14306.

    Article  PubMed  Google Scholar 

  26. Augustyn A, Borromeo M, Wang T, Fujimoto J, Shao C, Dospoy PD, Lee V, Tan C, Sullivan JP, Larsen JE, Girard L, Behrens C, Wistuba II, Xie Y, Cobb MH, Gazdar AF, Johnson JE, Minna JD. ASCL1 is a lineage oncogene providing therapeutic targets for high-grade neuroendocrine lung cancers. Proc Natl Acad Sci U S A. 2014;111:14788–93. https://doi.org/10.1073/pnas.1410419111.

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  27. Higashiyama M, Doi O, Kodama K, Yokouchi H, Tateishi R. High prevalence of bcl-2 oncoprotein expression in small cell lung cancer. Anticancer Res. 1995;15:503–5.

    CAS  PubMed  Google Scholar 

  28. Chau NG, Ma C, Danga K, Al-Sayegh H, Nardi V, Barrette R, Lathan CS, DuBois SG, Haddad RI, Shapiro GI, Sallan SE, Dhar A, Nelson JJ, French CA. An anatomical site and genetic-based prognostic model for patients with nuclear protein in testis (NUT) midline carcinoma: analysis of 124 patients. JNCI Cancer Spectr. 2020;4:pkz094. https://doi.org/10.1093/jncics/pkz094.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

The authors thank M. Iwakoshi, T. Kakita, S. Baba, Y. Togashi and H. Nagano for technical assistance. We would also like to thank Enago (www.enago.jp) for the English language review.

Research involving human participants and/or animals

In compliance with ethical standards, our study involving human participants was conducted following the guidelines outlined in the Declaration of Helsinki. The research protocol was approved by the Institutional Review Board (IRB) of Cancer Institute, Japanese Foundation for Cancer Research.

Data privacy

Despite the waiver of informed consent, all personal data were handled with strict confidentiality and in accordance with data protection regulations.

Funding

Kentaro Inamura received Grants-in-Aids for Scientific Research (Kakenhi) (#: 19K07426) from the Japan Society for the Promotion of Science (JSPS). Yuichi Ishikawa received Grants-in-Aids for Scientific Research (Kakenhi) from the Japan Society for the Promotion of Science (JSPS) (grant #: 19H03446), grants from the Japan Agency for Medical Research and Development (AMED), funding for mesothelioma projects entrusted by the Ministry of Environment, and is a consultant for Fujirebio Inc.

Author information

Authors and Affiliations

  1. Division of Pathology, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan

    Hironori Ninomiya, Yukiko Sato, Kentaro Inamura, Kengo Takeuchi & Yuichi Ishikawa

  2. Department of Pathology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan

    Hironori Ninomiya, Yukiko Sato, Kentaro Inamura & Kengo Takeuchi

  3. Pathology Project for Molecular Targets, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan

    Akito Dobashi & Kengo Takeuchi

  4. Division of Head and Neck Surgery, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan

    Hiroki Mitani

  5. Thoracic Surgical Oncology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan

    Mingyon Mun

  6. Thoracic Medical Oncology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan

    Makoto Nishio

  7. Department of Pathology, Mita Hospital, International University of Health and Welfare, Tokyo, Japan

    Yuichi Ishikawa

Authors
  1. Hironori Ninomiya
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Yukiko Sato
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Kentaro Inamura
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Akito Dobashi
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Kengo Takeuchi
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Hiroki Mitani
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Mingyon Mun
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Makoto Nishio
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Yuichi Ishikawa
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

H.N. conceived and designed the study, conducted experiments, and analyzed data. Y.S. contributed to data analysis and interpretation, as well as manuscript preparation. K.I. assisted in manuscript writing. K.T. contributed to the data interpretation and revision of the manuscript. H.M. contributed to the revision of the manuscript. M.M. contributed to the revision of the manuscript. M.N. contributed to the revision of the manuscript. Y.I. supervised the study and provided critical feedback on the manuscript.

Corresponding author

Correspondence to Hironori Ninomiya.

Ethics declarations

Ethics approval and consent to participate

This study involved human participants but was granted a waiver for the requirement of informed consent due to retrospective analysis of anonymized data. The study was conducted in accordance with the ethical standards of the institutional review board at the JFCR, and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The approval number is [JFCR (#2012–1042)].

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ninomiya, H., Sato, Y., Inamura, K. et al. Neuroendocrine and squamous cell phenotypes of NUT carcinoma are potential diagnostic pitfalls that discriminating it from mimickers, such as small cell and squamous cell carcinoma. Diagn Pathol 19, 27 (2024). https://doi.org/10.1186/s13000-024-01448-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13000-024-01448-7

Keywords

Diagnostic Pathology

ISSN: 1746-1596

Contact us