Open Access

Effects of radioactive 125I on apoptosis of HGC-27 gastric cancer cells

  • Authors:
    • Yong Yang
    • Aifei Chen
    • Jun Ma
    • Aiping Wu
    • Fazhen Xu
  • View Affiliations

  • Published online on: September 9, 2019     https://doi.org/10.3892/ol.2019.10832
  • Pages: 4916-4922
  • Copyright: © Yang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Effects of radioactive 125I particles at different doses on apoptosis of HGC-27 gastric cancer cells were investigated. HGC-27 gastric cancer cell suspension was used to establish a tumor-bearing mouse model. The model was reared for approximately 3 weeks and then divided into the control group (implanted with blank particles), the low dose group (implanted with 1.48x10-7 Bq 125I particles), the medium dose group (implanted with 2.22x10-7 Bq 125I particles) and the high dose group (implanted with 2.96x10-7 Bq 125I particles) (n=15 per group). Six nude mice were randomly sacrificed to collect the tumor tissue and measure tumor volume and mass. TUNEL (TdT-mediated dUTP nick-end labeling) was used for detecting apoptosis of tumor cells, and reverse transcription-quantitative polymerase chain reaction (RT-qPCR) for detecting the relative expression of Bax, caspase-3 and caspase-8. On the 28th day after implantation, the apoptotic rate in the low, medium and high dose groups was significantly higher than that in the control group, which in the medium and high dose groups was significantly lower than that in the low dose group (P<0.05). On the 28th day after implantation, the relative expression of Bax, caspase-3 and caspase-8 mRNA in the control group was significantly lower than that in the low, medium and high dose groups (P<0.05), which in the low dose group was significantly higher than that in the medium and high dose groups (P<0.05). 125I particles can inhibit the growth of HGC-27 gastric cancer cell transplants and promote the expression of Bax, caspase-3 and caspase-8 mRNA in the tumor tissue. Low-dose 125I particles are significantly more effective than medium- or high-dose 125I particles.

Introduction

Malignant tumors are recognized worldwide as public health and safety issues. Global cancer statistics in 2012 showed that gastric cancer was clinically common, and cancer statistics in China showed that there were 679,100 new patients and 498,000 deaths in 2015. The high incidence and mortality rates of the disease need to be urgently reduced (13). Operation, the best way to clinically treat cancer, improves conditions through excising the focal zone. However, early gastric cancer shows no obvious abnormalities, and patients are admitted to hospital after they feel unwell. As a result, most patients miss the best treatment time and can only be conservatively treated to alleviate conditions (4,5).

Therapeutic regimens for cancer have been increasing with the improvement of medical levels and technology. External radiotherapy combined with chemotherapy which has been widely used in the treatment of the middle and advanced stages of cancer effectively prolongs the survival time of patients. However, toxic and side effects easily occur during the treatment, and the patients may even suffer from organ failure (6,7). According to a recent study, as a new and effective adjuvant treatment for tumors and a new option especially for patients with poor efficacy of traditional chemotherapy regimens, interstitial irradiation causes a small trauma to the body and has an appropriate radiation radius to accurately treat the local area of lesions (8). 125I is the main particle of internal radiotherapy and effective in the treatment of lung, prostate, pancreatic, rectal and gastric cancer (911). However, its specific mechanism on inhibiting tumor growth remains unclear. Apoptosis, which is an important means of the clinical treatment of tumors, refers to the autonomous and orderly death of cells controlled by genes in order to maintain homeostasis (12).

Therefore, the mechanism of 125I on anti-apoptosis of gastric cancer HGC-27 cells was explored in this study to provide a reference for clinical treatment.

Materials and methods

Animal sources

Sixty male SPF (specific pathogen free) nude mice BALB/c (Beijing Vital River Laboratory Animal Technology Co., Ltd., weighing 20±2 g and aged 4 weeks, were reared by professionals for 1 week after being purchased. The indoor temperature was 21±2°C, the indoor humidity was 50–70%, with 12-h light/dark cycles and free access to food and water.

The study was approved by the Ethics Committee of Huaian TCM Hospital Affiliated to Nanjing University of Chinese Medicine (Huaian, China).

Main reagents and instruments

HGC-27 cells (Elabscience Biotechnology Inc., CL-0107), 125I particles (Tianjin Xiehe Medicine Technology Group Co., Ltd.), RPMI-1640 medium culture solution, 10% fetal bovine serum (FBS), penicillin-streptomycin (antibiotics) and TRIzol extraction reagent [Thermo Fisher Scientific (China) Co., Ltd., 61870044, 10099141, 15070063, 16096020], TransScript Two-Step RT-PCR SuperMix kit (TransGen Biotech, AT411-02). Primers for Bax, caspase-3, caspase-8 and GAPDH PCR (Table I) were designed and synthesized by Sangon Biotech (Shanghai) Co., Ltd. TUNEL apoptosis detection kit (Beyotime Biotechnology, C1091), PCR instrument (Applied Biosystems; Thermo Fisher Scientific, Inc., 7500).

Table I.

Primer sequences.

Table I.

Primer sequences.

GenesUpstream primersDownstream primers
Bax 5′-GGGTTGTCGCCCTTTTCTAC-3′ 5′-GGTGAGGAGGCTTGAGGAGT-3′
Caspase-3 5′-AAGGCAGAGCCATGGACCAC-3′ 5′-CTGGCAGCATCATCCACACATAC-3′
Caspase-8 5′-GTTCTCTCAGTTGCCTTTC-3′ 5′-AGCTGTAACCTGTCGCCGAGTCCC-3′
GAPDH 5′-GCACCGTCAAGGCTGAGAAC-3′ 5′-TGGTGAAGACGCCAGTGGA-3′
Cell culture

HCG-27 cells were resuscitated, transferred to the RPMI-1640 medium culture solution (containing 10% FBS, penicillin-streptomycin), and then cultured in an incubator (37°C, 5% CO2) for 2–3 days. After that, passage was performed. Cells in logarithmic growth phase were prepared into 1×106 cells/ml cell suspension using PBS buffer in order to establish an animal model.

Animal modeling and grouping

The cell suspension was inoculated into the subcutaneous side of the left back near the head of nude mice, reared by professionals for 3 weeks under SPF conditions. Subsequent experiments were performed after neoplasia. Sixty nude mice were randomized into the control group (blank particles), the low dose group (1.48×10−7 Bq 125I particles), the medium dose group (2.22×10−7 Bq 125I particles) and the high dose group (2.96×10−7 Bq 125I particles) (n=15 per group). According to the principles of aseptic technique, a needle for particle implantation was implanted into the central region of the tumor based on the tumor diameter. After 4 weeks of implantation under SPF conditions, the nude mice in groups were separately reared in cages to avoid mutual biting.

Detection of tumor volume and mass

Six nude mice were randomly anesthetized with 10% chloral hydrate (350 mg/kg) by intraperitoneal injection and then sacrificed by cervical dislocation before implantation (day 0) and on the 7th, 14th, 21st and 28th day after implantation, respectively, in order to collect the tumor tissue and measure tumor volume and mass [Tumor volume = long diameter (mm) × short diameter (mm2)/2].

Detection of apoptotic rate

After being anesthetized with 10% chloral hydrate (350 mg/kg) and then sacrificed by cervical dislocation, on the 28th day after implantation, the tumor tissue of nude mice was collected, fixed with 4% paraformaldehyde, dehydrated with gradient ethanol, embedded with paraffin, and finally sectioned. The TUNEL (TdT-mediated dUTP nick-end labeling) apoptosis detection kit was used for detecting apoptosis of tumor cells, with the operation carried out in strict accordance with the kit instructions. After staining, the apoptotic cells in the visual field were observed and counted using an optical microscope (×400; Olympus). The apoptotic rate = total number of apoptotic cells / total number of cells × 100%. After nuclear staining, the nuclei of normal tumor cells were blue, but those of apoptotic tumor cells were yellow or brownish yellow. Five visual fields of each section were randomly observed.

Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) detection. After being anesthetized with 10% chloral hydrate (350 mg/kg) and then sacrificed by cervical dislocation, the tumor tissue of nude mice on the 28th day after implantation was collected. The TRIzol extraction reagent was used for extracting total RNA, ultraviolet spectrophotometer (BioRad) and agarose gel electrophoresis for detecting its purity, concentration and integrity. Of the total RNA, 1 µg was reverse transcribed using 5X TransScript® II All-in-One SuperMix for PCR, with operations carried out in strict accordance with the manufacturer's kit. PCR amplification experiments were performed using the TransScript Two-Step SYBR-Green RT-PCR SuperMix kit, and the system was as follows: 1 µl of cDNA, each 0.5 µl of upstream and downstream primers, 12.5 µl of 2X TransTaq® HiFi PCR SuperMix II, and finally Nechelase-free Water was added to total of 25 µl. Conditions were as follows: pre-denaturation at 94°C for 5 min, denaturation at 94°C for 30 sec, annealing at 60°C for 30 sec, extension at 72°C for 30 sec, for 40 cycles. Three identical wells were set for each sample and the experiment was performed 3 times. GAPDH was used as an internal reference, and 2−∆∆cq was used to analyze the data (13).

Statistical analysis

In this study, SPSS20.0 software package (Guangzhou Pomine Information Technology Co., Ltd.) was used for statistically analyzing the data, GraphPad Prism 7 (Cabit Information Technology Co., Ltd.) for plotting the figures. Measurement data were expressed as mean ± standard deviation (mean ± SD), and comparison between two groups was tested by independent samples t-test and represented by t. Analysis of variance was used for comparison between groups, LSD-t test for pairwise comparison after that. P<0.05 was considered to indicate a statistically significant difference.

Results

Modeling

Sixty nude mice were subjected to tumorigenicity experiments, and no mouse died during the modeling.

Comparison of tumor volume

In this study, there was no significant difference in the tumor volume between the groups before implantation (P>0.05). On the 7th day after implantation, the tumor volume in the low, medium and high dose groups was significantly lower than that in the control group (P<0.05); there was no difference between the low and medium dose groups (P>0.05); the tumor volume in the low and medium dose groups was significantly lower than that in the high dose group (P<0.05). On the 14th day after implantation, the tumor volume in the low, medium and high dose groups was significantly lower than that in the control group (P<0.05), which in the medium dose group was significantly higher than that in the high dose group (P<0.05); there was no significant difference between the other groups (P>0.05). On the 21st day after implantation, the tumor volume in the low, medium and high dose groups was significantly lower than that in the control group (P<0.05); there was no difference between the other groups (P>0.05). On the 28th day after implantation, the tumor volume in the low, medium and high dose groups was significantly lower than that in the control group (P<0.05), which in the low dose group was significantly lower than that in the medium and high dose groups (P<0.05); there was no difference between the other groups (P>0.05). The comparison in the group showed that the tumor volume in the control group gradually increased with time, while that in the low, medium and high dose groups gradually decreased with time. In the control group, there was a significant difference between day 0 and on the 14th, 21st, 28th day (P<0.05); there was no significant difference between the other two time-points (P>0.05). In the low dose group, there was no significant difference between the 14th day and the 21st day (P>0.05); there was a significant difference between the other time-points (P<0.05). In the medium dose group, there was a statistically significant difference between each time-point (P<0.05). In the high dose group, there was no difference between day 0 and the 7th day, as well as between the 14th day and 21st day (P>0.05); there was a significant difference between the other time-points (P<0.05) (Table II).

Table II.

Comparison of tumor volume (mm3).

Table II.

Comparison of tumor volume (mm3).

GroupsBefore implantation (Day 0)7th day after implantation14th day after implantation21st day after implantation28th day after implantation
Control group (n=6)548.7±24.5580.1±24.5 605.4±16.2a 609.5±22.7a 608.8±24.5a
Low dose group (n=6, 1.48×10−7 Bq 125I)551.4±24.1 475.4±20.1a,e 357.1±16.7a,b,e 325.6±15.1a,b,e 230.1±14.2ae
Medium dose group (n=6, 2.22×10−7 Bq 125I)550.1±24.4 461.2±17.3a,e 361.5±20.1a,b,e 329.1±20.2ac,e 270.2±19.2af
High dose group (n=6, 2.96×10−7 Bq 125I)557.1±21.6540.1± 19.3eg 330.1±22.2a,b,e,g 331.0±17.5a,b,e 261.3±15.7af

a P<0.05 indicates a difference compared with before implantation

b P<0.05 indicates a difference compared with the 7th day after implantation

c P<0.05 indicates a difference compared with the 14th day after implantation.

d P<0.05 indicates a difference compared with the 21st day after implantation

e P<0.05 indicates a difference compared with the control group

f P<0.05 indicates a difference compared with the low dose group

g P<0.05 indicates that there is a difference compared with the medium dose group.

Comparison of tumor mass

There was no significant difference in the tumor mass between the groups before implantation (P>0.05). On the 7th day after implantation, the tumor mass in the low, medium and high dose groups was significantly lower than that in the control group (P<0.05); there was no difference between the other groups (P>0.05). On the 14th day after implantation, the tumor mass in the low, medium and high dose groups was significantly lower than that in the control group, which in the medium and high dose groups was significantly higher than that in the low dose group, and which in the high dose group was significantly lower than that in the medium dose group (P<0.05). On the 21st day after implantation, there was no difference in the tumor mass between the medium and high dose groups (P>0.05); the tumor mass in the low, medium and high dose groups was significantly lower than that in the control group, which in the medium and high dose groups was significantly higher than that in the control group (P<0.05). On the 28th day after implantation, the tumor mass in the low, medium and high dose groups was significantly lower than that in the control group, which in the medium and high dose groups was significantly higher than that in the low dose group, and which in the high dose group was significantly higher than that in the medium dose group (P<0.05). The comparison in the group showed that the tumor mass in the control group gradually increased with time, while that in the low, medium and high dose groups gradually decreased with time. In the control group, there was no significant difference between each time-point (P>0.05). In the low dose group, there was no significant difference between day 0 and on the 7th day (P>0.05); there was a significant difference between the other time-points (P<0.05). In the medium dose group, there was no significant difference between day 0 and the 7th day (P>0.05); there was a significant difference between the other time-points (P<0.05). In the high dose group, there was no significant difference between the 21st and 28th day (P>0.05); there was a significant difference between the other time-points (P<0.05) (Table III).

Table III.

Comparison of tumor mass (g).

Table III.

Comparison of tumor mass (g).

GroupsBefore implantation (Day 0)7th day after implantation14th day after implantation21st day after implantation28th day after implantation
Control group (n=6)2.032±0.0442.125±0.0732.131±0.0512.134±0.0512.137±0.066
Low dose group (n=6, 1.48×10−7 Bq 125I)2.030±0.061 1.968±0.060e 1.488±0.069a,b,e 1.015±0.041ac,e 0.686±0.050ae
Medium dose group (n=6, 2.22×10−7 Bq 125I)2.035±0.049 1.987±0.077e 1.815±0.062a,b,e,f 1.435±0.052ac,e,f 1.061±0.048af
High dose group (n=6, 2.96×10−7 Bq 125I)2.044±0.052 1.944±0.051a,e 1.752±0.070a,b,eg 1.384±0.067ac,e,f 1.185±0.052ac, eg

a P<0.05 indicates a difference compared with before implantation

b P<0.05 indicates a difference compared with the 7th day after implantation

c P<0.05 indicates a difference compared with the 14th day after implantation.

d P<0.05 indicates a difference compared with the 21st day after implantation

e P<0.05 indicates a difference compared with the control group

f P<0.05 indicates a difference compared with the low dose group

g P<0.05 indicates that there is a difference compared with the medium dose group.

Comparison of apoptosis

On the 28th day after implantation, there was a significant difference in the apoptotic rate between the groups (P<0.001). The apoptotic rate in the low, medium and high dose groups was significantly higher than that in the control group, which in the medium and high dose groups was significantly lower than that in the low dose group (P<0.001). There was no difference between other groups (P>0.05) (Table IV, Fig. 1).

Table IV.

Apoptotic rates on the 28th day.

Table IV.

Apoptotic rates on the 28th day.

GroupsApoptotic rate on the 28th day (%)
Control group (n=6)7.24±1.78
Low dose group (n=6, 1.48×10−7 Bq 125I) 45.22±5.97a
Medium dose group (n=6, 2.22×10−7 Bq 125I) 35.12±4.22a,b
High dose group (n=6, 2.96×10−7 Bq 125I) 40.54±4.35a,b
F value92.188
P-value<0.001

a P<0.05 indicates a difference compared with the control group

b P<0.05 indicates a difference compared with the low dose group.

Comparison of Bax, caspase-3 and caspase-8 mRNA

On the 28 day after implantation, the relative expression of Bax, caspase-3 and caspase-8 mRNA in the control group was significantly lower than that in the low, medium and high dose groups (P<0.05), which in the low dose group was significantly higher than that in the medium and high dose groups (P<0.05). There was no significant difference between the medium and high dose groups (P>0.05) (Table V, Fig. 2).

Table V.

Comparison of Bax, caspase-3 and caspase-8 mRNA on the 28th day.

Table V.

Comparison of Bax, caspase-3 and caspase-8 mRNA on the 28th day.

GroupsBaxCaspase-3Caspase-8
Control group (n=6)1.035±0.0411.024±0.0321.028±0.030
Low dose group (n=6) 1.892±0.174a 2.522±0.301a 2.122±0.170a
Medium dose group (n=6) 1.641±0.120a,b 1.891±0.260a,b 1.715±0.121a,b
High dose group (n=6) 1.705±0.081a,b 1.755±0.217a,b 1.658±0.148a,b
F value62.46143.96273.853
P-value<0.001<0.001<0.001

a P<0.05, a difference compared with the control group

b P<0.05, a difference compared with the low dose group.

Discussion

Gastric cancer is a common malignant disease in the clinical department of gastroenterology and oncology. A cancer statistics report in the United States showed that there were 28,000 new patients and 15,700 deaths in 2017 (14). The disease is usually caused by changes in dietary habits, Helicobacter pylori infection, genetics and socioeconomic status among which the first one is the most common cause. Irregular diet, alcohol abuse, and lack of trace elements in daily diet lead to an increase in the incidence rate of the disease (15,16). At present, gastric cancer is clinically treated by operation, but most patients after admission are in the middle and advanced stages of the disease and have missed the best treatment time, so they cannot be treated by operation (17). Radiotherapy, as an important means of the clinical treatment of cancer, has been widely used. According to a study, the survival time of patients with local advanced esophageal and gastric cancer after radiotherapy was significantly increased (18). However, traditional radiotherapy leads to necrosis in the normal tissue other than the lesion tissue during the treatment, and excessive radiation increases adverse reactions.

Internal radiotherapy has been gradually recognized by clinicians as medical technology continues to be improved, and its adjuvant treatment of malignant tumors has been widely used in clinical practice. 125I is a synthetic isotope and has a long half-life (60.1d). Compared with traditional radiotherapy, it has a more appropriate radiation radius to accurately treat the local area of lesions, and causes less trauma and damage to the normal tissue adjacent to lesions (19). In a study by Shi et al (20), the implantation of 125I particles in patients with recurrent colorectal cancer significantly prolonged the survival time of the patients (21). In a study by Jiang et al (21), 56 lesions were treated through the implantation in patients with gastrointestinal cancer with pulmonary metastasis, with an overall local control rate of 91.1%. These findings indicate that the transplantation of 125I particles effectively inhibits tumor growth. Currently, clinical radiotherapy and chemotherapy affect tumor growth mainly through promoting tumor apoptosis (22). How do 125I particles affect apoptotic factors in gastric cancer? Effects of radioactive 125I on apoptosis at different doses in gastric cancer cells were investigated. In this study, a tumor-forming mouse model was established to observe the effects of radioactive 125I particles at different doses on the tumor tissue, so as to provide a reference for clinical practice.

The proliferation of tumors is an important factor determining their growth rates. A tumor-forming mouse model was successfully established. The tumor volume and mass of nude mice in the low, medium and high groups gradually decreased with time, suggesting that 125I particles can effectively inhibit the growth of gastric cancer tumors, probably because 125I radiation directly destroys the DNA double strands of tumor cells and activates the expression of apoptotic factors in cells, thereby inducing apoptosis (23). Therefore, the apoptotic factors of gastric cancer tumors in nude mice were detected on the 28th day. Bax is a classical pro-apoptotic factor in the Bcl-2 family and lowly expressed in cells, and its expression is significantly increased when cells undergo apoptosis (24). Caspase-3 and caspase-8 belong to the Caspase family; Caspase-8 plays an important role in the activation of apoptosis and caspase-3 playing an important role during apoptosis (25). A study shows that the activation of them promotes apoptosis (26). In this study, on the 28th day after implantation, the relative expression of Bax, caspase-3 and caspase-8 mRNA in the low, medium and high groups was significantly higher than that in the control group, which indicates that 125I particles can promote expression of Bax, caspase-3 and caspase-8 mRNA in gastric cancer tumors and thereby promote apoptosis. According to TUNEL, apoptosis in the low, medium and high groups was significantly higher than that in the control group. Sun et al (27) treated patients with stage IIIB-IV lung cancer by EGFR-TKI combined with the implantation of 125I particles, and the expression of Bax in the tissue of the patients was significantly increased 1 month later. In a study by Wang et al (28), compared with high-dose 60Co, the expression of Bax and caspase-3 was significantly increased after low-dose 125I radiation to lung cancer cells A549 and H1299.

In a study by Chen and Wang (29), the expression of caspase-8 was significantly increased through 125I irradiation to a rat model of glioma. In HGC-27 gastric cancer cell transplants in nude mice, 125I particles effectively increased the expression of Bax, caspase-3 and caspase-8 mRNA in gastric cancer tumors, indicating that 125I particles can increase the expression of Bax, caspase-3 and caspase-8 mRNA in tumor cells and promote apoptosis. However, on the 28th day after implantation, the tumor volume and mass in the low dose group were significantly lower than those in the medium and high dose groups, while the expression of Bax, caspase-3, caspase-8 mRNA and apoptosis were significantly higher than those in the medium and high dose groups. These findings suggest that low-dose 125I particles are significantly more effective than medium- and high-dose 125I particles in inhibiting the growth of gastric cancer tumors. In a study by Lehmann and Dröge (30), the apoptotic rate of HeLa cells after 5 Gy 125I irradiation was significantly higher than that after 10 Gy 125I irradiation. The above is similar to the results of our study, possibly because tumor cells increase their own adaptability and protection during the growth in order to avoid the toxic effects of radiation, resulting in resistance which is often referred to as the inverse dosage effect (31).

The present study showed that low-dose 125I was significantly more effective than medium- and high-dose 125I in inhibiting the growth of HGC-27 gastric cancer cell transplants. However, there are still deficiencies. This animal experiment was not clinically verified, and the expression of Bax, caspase-3 and caspase-8 mRNA at other time-points was not detected. Thus further confirmational studies are required.

In summary, 125I particles can inhibit the growth of HGC-27 gastric cancer cell transplants, and promote the expression of Bax, caspase-3 and caspase-8 mRNA in the tumor tissue. Low-dose 125I particles are significantly more effective than medium- and high-dose 125I particles.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.

Authors' contributions

YY wrote the manuscript. YY and AC were responsible for animal modeling. JM and AW performed PCR and TUNEL assay. FX contributed to detection of tumor volume and mass. All the authors read and approved the final manuscript.

Ethics approval and consent to participate

The study was approved by the Ethics Committee of Huaian TCM Hospital Affiliated to Nanjing University of Chinese Medicine (Huaian, China).

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References

1 

Torre LA, Bray F, Siegel RL, Ferlay J, Lortet-Tieulent J and Jemal A: Global cancer statistics, 2012. CA Cancer J Clin. 65:87–108. 2015. View Article : Google Scholar : PubMed/NCBI

2 

Rahib L, Smith BD, Aizenberg R, Rosenzweig AB, Fleshman JM and Matrisian LM: Projecting cancer incidence and deaths to 2030: The unexpected burden of thyroid, liver, and pancreas cancers in the United States. Cancer Res. 74:2913–2921. 2014. View Article : Google Scholar : PubMed/NCBI

3 

Chen W, Zheng R, Baade PD, Zhang S, Zeng H, Bray F, Jemal A, Yu XQ and He J: Cancer statistics in China, 2015. CA Cancer J Clin. 66:115–132. 2016. View Article : Google Scholar : PubMed/NCBI

4 

Kim W, Kim HH, Han SU, Kim MC, Hyung WJ, Ryu SW, Cho GS, Kim CY, Yang HK, Park DJ, et al Korean Laparo-endoscopic Gastrointestinal Surgery Study (KLASS) Group, : Decreased morbidity of laparoscopic distal gastrectomy compared with open distal gastrectomy for stage I gastric cancer: Short-term outcomes from a multicenter randomized controlled trial (KLASS-01). Ann Surg. 263:28–35. 2016. View Article : Google Scholar : PubMed/NCBI

5 

Li P, Chen S, Chen H, Mo X, Li T, Shao Y, Xiao B and Guo J: Using circular RNA as a novel type of biomarker in the screening of gastric cancer. Clin Chim Acta. 444:132–136. 2015. View Article : Google Scholar : PubMed/NCBI

6 

Obi N, Eulenburg C, Seibold P, Eilber U, Thöne K, Behrens S, Chang-Claude J and Flesch-Janys D: Associations between adjuvant radiotherapy and different causes of death in a German breast cancer cohort. Breast. 38:75–80. 2018. View Article : Google Scholar : PubMed/NCBI

7 

Manocha R, Marks GB, Kenchington P, Peters D and Salome CM: Sahaja yoga in the management of moderate to severe asthma: A randomised controlled trial. Thorax. 57:110–115. 2002. View Article : Google Scholar : PubMed/NCBI

8 

Vilgrain V, Pereira H, Assenat E, Guiu B, Ilonca AD, Pageaux GP, Sibert A, Bouattour M, Lebtahi R, Allaham W, et al SARAH Trial Group, : Efficacy and safety of selective internal radiotherapy with yttrium-90 resin microspheres compared with sorafenib in locally advanced and inoperable hepatocellular carcinoma (SARAH): An open-label randomised controlled phase 3 trial. Lancet Oncol. 18:1624–1636. 2017. View Article : Google Scholar : PubMed/NCBI

9 

Huo X, Wang H, Yang J, Li X, Yan W, Huo B, Zheng G, Chai S, Wang J, Guan Z, et al: Effectiveness and safety of CT-guided (125)I seed brachytherapy for postoperative locoregional recurrence in patients with non-small cell lung cancer. Brachytherapy. 15:370–380. 2016. View Article : Google Scholar : PubMed/NCBI

10 

Kittel JA, Reddy CA, Smith KL, Stephans KL, Tendulkar RD, Ulchaker J, Angermeier K, Campbell S, Stephenson A, Klein EA, et al: Long-term efficacy and toxicity of low-dose-rate 125I prostate brachytherapy as monotherapy in low-, intermediate-, and high-risk prostate cancer. Int J Radiat Oncol Biol Phys. 92:884–893. 2015. View Article : Google Scholar : PubMed/NCBI

11 

Wang GC, Liu F, Xie TH, Liu FL and Zhang CQ: Combined intestinal and biliary stenting in gastric outlet and biliary obstruction. Gastroenterology Res. 2:29–34. 2009.PubMed/NCBI

12 

Chen K, Li G, Geng F, Zhang Z, Li J, Yang M, Dong L and Gao F: Berberine reduces ischemia/reperfusion-induced myocardial apoptosis via activating AMPK and PI3K-Akt signaling in diabetic rats. Apoptosis. 19:946–957. 2014. View Article : Google Scholar : PubMed/NCBI

13 

Livak KJ and Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods. 25:402–408. 2001. View Article : Google Scholar : PubMed/NCBI

14 

Siegel RL, Miller KD and Jemal A: Cancer statistics, 2017. CA Cancer J Clin. 67:7–30. 2017. View Article : Google Scholar : PubMed/NCBI

15 

Karimi P, Islami F, Anandasabapathy S, Freedman ND and Kamangar F: Gastric cancer: Descriptive epidemiology, risk factors, screening, and prevention. Cancer Epidemiol Biomarkers Prev. 23:700–713. 2014. View Article : Google Scholar : PubMed/NCBI

16 

Plummer M, Franceschi S, Vignat J, Forman D and de Martel C: Global burden of gastric cancer attributable to Helicobacter pylori. Int J Cancer. 136:487–490. 2015. View Article : Google Scholar : PubMed/NCBI

17 

Neugut AI, Hayek M and Howe G: Epidemiology of gastric cancer. Semin Oncol. 23:281–291. 1996.PubMed/NCBI

18 

Katai H, Mizusawa J, Katayama H, Takagi M, Yoshikawa T, Fukagawa T, Terashima M, Misawa K, Teshima S, Koeda K, et al: Short-term surgical outcomes from a phase III study of laparoscopy-assisted versus open distal gastrectomy with nodal dissection for clinical stage IA/IB gastric cancer: Japan Clinical Oncology Group Study JCOG0912. Gastric Cancer. 20:699–708. 2017. View Article : Google Scholar : PubMed/NCBI

19 

Ng J and Lee P: The role of radiotherapy in localized esophageal and gastric cancer. Hematol Oncol Clin North Am. 31:453–468. 2017. View Article : Google Scholar : PubMed/NCBI

20 

Shi L, Li X, Pei H, Zhao J, Qiang W, Wang J, Xu B, Chen L, Wu J, Ji M, et al: Phase II study of computed tomography-guided (125)I-seed implantation plus chemotherapy for locally recurrent rectal cancer. Radiother Oncol. 118:375–381. 2016. View Article : Google Scholar : PubMed/NCBI

21 

Jiang Y, Huang ZL, Wu PH, Zhang FJ, Zhao M, Huang JH, Fan WJ, Li CX, Gu YK, Zhang L, et al: Short-term efficacy of ct-guided radioactive seed 125I implantation on residual or relapsing metastatic lymph nodes in advanced tumor patients after multi-modality treatment. Ai Zheng. 27:1082–1087. 2008.(In Chinese). PubMed/NCBI

22 

Xie L, Chen Y, Zhang Y, Yang Z, Zhang Z, Shen L, Yuan Z and Ren M: Status and prospects of percutaneous vertebroplasty combined with 125I seed implantation for the treatment of spinal metastases. World J Surg Oncol. 13:1192015. View Article : Google Scholar : PubMed/NCBI

23 

Safarzadeh E, Sandoghchian Shotorbani S and Baradaran B: Herbal medicine as inducers of apoptosis in cancer treatment. Adv Pharm Bull. 4 (Suppl 1):421–427. 2014.PubMed/NCBI

24 

Chen W, Kang J, Xia J, Li Y, Yang B, Chen B, Sun W, Song X, Xiang W, Wang X, et al: p53-related apoptosis resistance and tumor suppression activity in UVB-induced premature senescent human skin fibroblasts. Int J Mol Med. 21:645–653. 2008.PubMed/NCBI

25 

Pu X, Storr SJ, Zhang Y, Rakha EA, Green AR, Ellis IO and Martin SG: Caspase-3 and caspase-8 expression in breast cancer: Caspase-3 is associated with survival. Apoptosis. 22:357–368. 2017. View Article : Google Scholar : PubMed/NCBI

26 

Dubey M, Nagarkoti S, Awasthi D, Singh AK, Chandra T, Kumaravelu J, Barthwal MK and Dikshit M: Nitric oxide-mediated apoptosis of neutrophils through caspase-8 and caspase-3-dependent mechanism. Cell Death Dis. 7:e23482016. View Article : Google Scholar : PubMed/NCBI

27 

Sun W, Yuan X, Tian Y, Wu H, Xu H, Hu G and Wu K: Non-invasive approaches to monitor EGFR-TKI treatment in non-small-cell lung cancer. J Hematol Oncol. 8:952015. View Article : Google Scholar : PubMed/NCBI

28 

Wang Z, Zhao Z, Lu J, Chen Z, Mao A, Teng G and Liu F: A comparison of the biological effects of 125I seeds continuous low-dose-rate radiation and 60Co high-dose-rate gamma radiation on non-small cell lung cancer cells. PLoS One. 10:e01337282015. View Article : Google Scholar : PubMed/NCBI

29 

Chen F and Wang D: Inhibition of glioblastoma growth and invasion by 125I brachytherapy in rat glioma model. Am J Transl Res. 9:2243–2254. 2017.PubMed/NCBI

30 

Lehmann V and Dröge W: Demonstration of membrane receptors for human natural and recombinant 125I-labeled tumor necrosis factor on HeLa cell clones and their role in tumor cell sensitivity. Eur J Biochem. 158:1–5. 1986. View Article : Google Scholar : PubMed/NCBI

31 

Ling CC, Gerweck LE, Zaider M and Yorke E: Dose-rate effects in external beam radiotherapy redux. Radiother Oncol. 95:261–268. 2010. View Article : Google Scholar : PubMed/NCBI

Related Articles

Journal Cover

November-2019
Volume 18 Issue 5

Print ISSN: 1792-1074
Online ISSN:1792-1082

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Yang Y, Chen A, Ma J, Wu A and Xu F: Effects of radioactive 125I on apoptosis of HGC-27 gastric cancer cells. Oncol Lett 18: 4916-4922, 2019
APA
Yang, Y., Chen, A., Ma, J., Wu, A., & Xu, F. (2019). Effects of radioactive 125I on apoptosis of HGC-27 gastric cancer cells. Oncology Letters, 18, 4916-4922. https://doi.org/10.3892/ol.2019.10832
MLA
Yang, Y., Chen, A., Ma, J., Wu, A., Xu, F."Effects of radioactive 125I on apoptosis of HGC-27 gastric cancer cells". Oncology Letters 18.5 (2019): 4916-4922.
Chicago
Yang, Y., Chen, A., Ma, J., Wu, A., Xu, F."Effects of radioactive 125I on apoptosis of HGC-27 gastric cancer cells". Oncology Letters 18, no. 5 (2019): 4916-4922. https://doi.org/10.3892/ol.2019.10832