Journal of Shandong University (Health Sciences) ›› 2024, Vol. 62 ›› Issue (4): 14-23.doi: 10.6040/j.issn.1671-7554.0.2024.0125

• Clinical Medicine • Previous Articles    

Expression of autophagy-related protein 5 in colon cancer and its impact on the migration and invasion ability of colon cancer cells

LIU Aijing1, LI Yanru1, GAO Huiru1, DUAN Weili1, LI Peilong1, LI Juan1, DU Lutao2, WANG Chuanxin1   

  1. 1. Department of Clinical Laboratory, The Second Hospital of Shandong University, Jinan 250033, Shandong, China;
    2. Department of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan 250012, Shandong, China
  • Published:2024-05-16

Abstract: Objective To evaluate the expression of autophagy-related protein 5(ATG5)in colon cancer and its relationship with clinicopathological features, and to analyze the effect of ATG5 on the migration and invasion ability of colon cancer cells. Methods The expression levels of ATG5 mRNA and ATG5 protein in colon cancer tissues and adjacent normal tissues were analyzed using the online analysis tool cProsite. Kaplan-Meier Plotter was used to analyze the effect of ATG5 expression level on the prognosis of colon cancer patients. The expression of ATG5 in 100 colon cancer tissues was detected by immunohistochemistry, and the correlation between the expression level of ATG5 and clinicopathological features was analyzed by χ2 and Fishers test. ATG5 was overexpressed or knocked down in colon cancer cells by transfecting plasmid or small interfering RNA(siRNA), and then the transfection efficiency and changes of microtubule-associated protein light chain 3(LC3)were detected by Western blotting. Transwell assay was used to evaluate migration and invasion ability of colon cancer cells after overexpression or knockdown. Differentially expressed genes associated with ATG5 in colon cancer were analyzed using the LinkedOmics database, and gene ontology(GO)and kyoto encyclopedia of genes and genomes(KEGG)enrichment analyses were performed. Results The expression levels of ATG5 mRNA and protein in colon cancer tissues were lower than those in adjacent normal tissues(P<0.001). The recurrence-free survival of colon cancer patients with low ATG5 expression was significantly shorter than those with high ATG5 expression(P<0.001). Immunohistochemistry showed that the expression level of ATG5 in colon cancer tissues was correlated with lymph node metastasis, and low expression of ATG5 in colon cancer patients was more likely to develop lymph node metastasis(P=0.027). Western blotting and Transwell experiments showed that after overexpression of ATG5 in SW1116 cells, the expression of LC3Ⅱ/LC3Ⅰ increased, and the migration and invasion ability of cells was weakened(PATG5=0.001; PLC3Ⅱ/LC3Ⅰ=0.04; Pmigration<0.001, Pinvasion<0.001). Conversely, ATG5 knockdown in DLD1 cells led to a decrease in the expression of LC3Ⅱ/LC3Ⅰ, and an increase in the migration and invasion ability of the cells(PATG5#1=0.021, PATG5#2<0.001; PLC3Ⅱ/LC3Ⅰ#1=0.013, PLC3Ⅱ/LC3Ⅰ#2=0.02; Pmigration<0.001, Pinvasion<0.001). ATG5-related differentially expressed gene enrichment analysis suggested that ATG5 might affect colon cancer metastasis by affecting DNA damage response, chromatin organization and Notch signaling pathway. Conclusion ATG5 is lowly expressed in colon cancer and is significantly correlated with lymph node metastasis and prognosis of patients. ATG5 in colon cancer cells can increase the level of autophagy and inhibit cell migration and invasion, suggesting that ATG5 and its regulated autophagy process may become a new target for the clinical treatment of colon cancer.

Key words: Autophagy-related protein 5, Tumor metastasis, Autophagy, Colon cancer, Microtubule-associated protein light chain 3

CLC Number: 

  • R735.3
[1] Sung H, Ferlay J, Siegel RL, et al. Global cancer statistics 2020: globocan estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J]. CA Cancer J Clin, 2021, 71(3): 209-249.
[2] 杨莹, 韩宇. 西妥昔单抗再挑战方案后线治疗晚期结直肠癌的研究进展[J]. 中国肿瘤, 2024, 33(2): 147-152. YANG Ying, HAN Yu. Research progress on the rechallenge with cetuximab regimen as post-line therapy for advanced colorectal cancer[J]. China Cancer, 2024, 33(2): 147-152.
[3] Hossain MS, Karuniawati H, Jairoun AA, et al. Colorectal cancer: a review of carcinogenesis, global epidemiology, current challenges, risk factors, preventive and treatment strategies[J]. Cancers(Basel), 2022, 14(7):1732. doi: 10.3390/cancers14071732.
[4] Gómez-Virgilio L, Silva-Lucero MD, Flores-Morelos DS, et al. Autophagy: a key regulator of homeostasis and disease: an overview of molecular mechanisms and modulators[J]. Cells, 2022, 11(15):2262. doi: 10.3390/cells11152262.
[5] Luo M, Ji J, Yang K, et al. The role of autophagy in the treatment of colon cancer by chlorin e6 photodynamic therapy combined with oxaliplatin[J]. Photodiagnosis Photodyn Ther, 2022, 40: 103082. doi: 10.1016/j.pdpdt.2022.103082.
[6] Jin X, You L, Qiao J, et al. Autophagy in colitis-associated colon cancer: exploring its potential role in reducing initiation and preventing IBD-related CAC development[J]. Autophagy, 2024, 20(2): 242-258.
[7] Zheng Y, Wu J, Chen H, et al. KLF4 targets RAB26 and decreases 5-FU resistance through inhibiting autophagy in colon cancer[J]. Cancer Biol Ther, 2023, 24(1): 2226353. doi: 10.1080/15384047.2023.2226353.
[8] Changotra H, Kaur S, Yadav SS, et al. ATG5: a central autophagy regulator implicated in various human diseases[J]. Cell Biochem Funct, 2022, 40(7): 650-667.
[9] Corkery DP, Castro-Gonzalez S, Knyazeva A, et al. An ATG12-ATG5-TECPR1 E3-like complex regulates unconventional LC3 lipidation at damaged lysosomes[J]. EMBO Rep, 2023, 24(9): e56841. doi: 10.15252/embr.202356841.
[10] Huang Q, Liu Y, Zhang S, et al. Autophagy core protein ATG5 is required for elongating spermatid development, sperm individualization and normal fertility in male mice[J]. Autophagy, 2021, 17(7): 1753-1767.
[11] Feng X, Zhang H, Meng L, et al. Hypoxia-induced acetylation of PAK1 enhances autophagy and promotes brain tumorigenesis via phosphorylating ATG5[J]. Autophagy, 2021, 17(3): 723-742.
[12] Yan J, Wang M, Lv S, et al. SiATG5-loaded cancer cell membrane-fused liposomes induced increased uptake of albumin-bound chemotherapeutics by pancreatic cancer cells[J]. J Control Release, 2024, 367: 620-636. doi: 10.1016/j.jconrel.2024.01.055.
[13] Hamada K, Kurashige T, Shimamura M, et al. MIEAP and ATG5 are tumor suppressors in a mouse model of BRAF(V600E)-positive thyroid cancer[J]. Front Endocrinol(Lausanne), 2022, 13: 932754. doi: 10.3389/fendo.2022.932754.
[14] Cao W, Li J, Yang K, et al. An overview of autophagy: mechanism, regulation and research progress[J]. Bull Cancer, 2021, 108(3): 304-322.
[15] Xing Y, Wei X, Liu Y, et al. Autophagy inhibition mediated by MCOLN1/TRPML1 suppresses cancer metastasis via regulating a ROS-driven TP53/p53 pathway[J]. Autophagy, 2022, 18(8): 1932-1954.
[16] Rangel M, Kong J, Bhatt V, et al. Autophagy and tumorigenesis[J]. FEBS J, 2022, 289(22): 7177-7198.
[17] Kao CH, Su TY, Huang WS, et al. TFEB- and TFE3-dependent autophagy activation supports cancer proliferation in the absence of centrosomes[J]. Autophagy, 2022, 18(12): 2830-2850.
[18] 李淑敏, 王之枫, 刘宗绪, 等. 细胞自噬调控在肿瘤中作用的研究进展[J]. 中国肿瘤临床, 2023, 50(19): 1006-1010. LI Shumin, WANG Zhifeng, LIU Zongxu, et al. Research progress on autophagy regulation in tumors[J]. Chinese Journal Clinical Oncology, 2023, 50(19): 1006-1010.
[19] Yang F, Peng ZX, Ji WD, et al. LncRNA CCAT1 upregulates ATG5 to enhance autophagy and promote gastric cancer development by absorbing miR-140-3p[J]. Dig Dis Sci, 2022, 67(8): 3725-3741.
[20] Yu Z, Tang H, Chen S, et al. Exosomal LOC85009 inhibits docetaxel resistance in lung adenocarcinoma through regulating ATG5-induced autophagy[J]. Drug Resist Updat, 2023, 67: 100915. doi: 10.1016/j.drup.2022.100915.
[21] Sprinzak D, Blacklow SC. Biophysics of notch signaling[J]. Annu Rev Biophys, 2021, 50: 157-189. doi: 10.1146/annurev-biophys-101920-082204.
[22] Suarez Rodriguez F, Sanlidag S, Sahlgren C. Mechanical regulation of the Notch signaling pathway[J]. Curr Opin Cell Biol, 2023, 85: 102244. doi: 10.1016/j.ceb.2023.102244.
[23] Qiu L, Yang X, Wu J, et al. HIST2H2BF potentiates the propagation of cancer stem cells via Notch signaling to promote malignancy and liver metastasis in colorectal carcinoma[J]. Front Oncol, 2021, 11: 677646. doi: 10.1016/j.ceb.2023.102244.
[24] Li X, Liu W, Geng C, et al. Ginsenoside Rg3 suppresses epithelial-mesenchymal transition via downregulating Notch-Hes1 signaling in colon cancer cells[J]. Am J Chin Med, 2021, 49(1): 217-235.
[25] Yoshida G, Kawabata T, Takamatsu H, et al. Degradation of the NOTCH intracellular domain by elevated autophagy in osteoblasts promotes osteoblast differentiation and alleviates osteoporosis[J]. Autophagy, 2022, 18(10): 2323-2332.
[26] Li Y, Ma L, Deng Y, et al. The Notch1/Hes1 signaling pathway affects autophagy by adjusting DNA methyltransferases expression in a valproic acid-induced autism spectrum disorder model[J]. Neuropharmacology, 2023, 239: 109682. doi: 10.1016/j.neuropharm.2023.109682.
[27] Rogers JM, Guo B, Egan ED, et al. MAML1-dependent Notch-responsive genes exhibit differing cofactor requirements for transcriptional activation[J]. Mol Cell Biol, 2020, 40(11): e00014-20. doi: 10.1128/MCB.00014-20.
[28] Yan X, Cheng Y, Zhang X, et al. NICD3 regulates the expression of MUC5AC and MUC2 by recruiting SMARCA4 and is involved in the differentiation of mucinous colorectal adenocarcinoma[J]. Mol Oncol, 2022, 16(19): 3509-3532.
[1] LIANG Yongyuan, CAI Peifei, ZHENG Guixi. Establishment and value assessment of colon cancer diagnostic models based on multiple variables and different machine learning algorithms [J]. Journal of Shandong University (Health Sciences), 2024, 62(2): 51-59.
[2] ZHENG Ronghui, Li Pan, CAO Xiuqin, HE Ruixia, CHEN Minjia, CHEN Haixia, YANG Zhiwei. SQSTM1 in Legionella pneumophila infected RAW264.7 cells mechanism of autophagy [J]. Journal of Shandong University (Health Sciences), 2023, 61(6): 10-21.
[3] REN Huixin, ZHENG Maojin, HAN Wencan, WANG Chaoqun, ZHOU Yun, PEI Dongsheng. Hydrogen peroxide enhances radiotherapy sensitivity of cervical cancer by regulating autophagy [J]. Journal of Shandong University (Health Sciences), 2023, 61(6): 22-28.
[4] HE Jing, YAN Rugen, WU Zhihong, LI Changzhong. Effects of Xiaozheng Yiai decoction on the proliferation and migration of ovarian cancer SKOV3 cells [J]. Journal of Shandong University (Health Sciences), 2023, 61(5): 1-10.
[5] XU Bing, LI Yong, LIU Ming, LIU Yonghui. Silencing PRRX1 gene expression enhances the sensitivity of prostate cancer resistant cell line PC-3/DTX to docetaxel [J]. Journal of Shandong University (Health Sciences), 2021, 59(6): 103-110.
[6] ZHANG Xiaohong, ZHOU Yun, DU Qiuying, REN Huixin, WANG Chaoqun. Atg7-siRNA interferes with radiosensitivity of esophageal cancer ECA109 cells by regulating arginine circulation [J]. Journal of Shandong University (Health Sciences), 2021, 59(4): 28-34.
[7] ZHEN Qiulai, LYU Xinran, YE Hui, DING Xuchao, CHAI Xiaoxue, HU Xin, ZHOU Ming, CAO Lili. Predicting colon cancer prognosis genes and clinical application value based on TCGA database [J]. Journal of Shandong University (Health Sciences), 2021, 59(1): 64-71.
[8] SUO Dongyang, SHEN Fei, GUO Hao, LIU Lichang, YANG Huimin, YANG Xiangdong. Expression and mechanism of Tim-3 in animal model of drug-induced acute kidney injury [J]. Journal of Shandong University (Health Sciences), 2020, 1(7): 1-6.
[9] SUN Panpan, ZHAO Xu, LIN Xiaowen, FU Zhijian. Effects of medical ozone on the expression of PPARγ and autophagy in chondrocytes of osteoarthritis in rats [J]. Journal of Shandong University (Health Sciences), 2020, 58(6): 14-21.
[10] SUN Wenkai, SUN Hui, WU Xinfang, GAO Wei, MENG Zhaotun, LI Qin. Expressions and clinical significance of Beclin-1, P62 and Ki67 in different parts of nasal polyps [J]. Journal of Shandong University (Health Sciences), 2020, 58(6): 76-82.
[11] ZHOU Jiahui, WANG Gang, LIU Jiang, ZHAO Jian, WANG Haifeng, JIANG Zhiwei. Effects of multimodal analgesia under the guidance of enhanced recovery after open surgery on postoperative recovery of patients with colon cancer [J]. Journal of Shandong University (Health Sciences), 2019, 57(9): 38-42.
[12] SUN Honglin, HAN Bo, WANG Jing, GAO Ling, ZHU Mei, JIANG Diandong, LÜ Jianli. Effects of c-Jun N-terminal kinase regulated by CD40siRNA on the autophagy of cardiomyocytes in rats with autoimmune myocarditis [J]. Journal of Shandong University (Health Sciences), 2019, 57(4): 9-14.
[13] GUAN Hongwei, LI Juan, SUN Rui, LIU Jie, LI Changzhong. Biological effects of ubenimex on ovarian cancer A2780 cell [J]. Journal of Shandong University (Health Sciences), 2019, 57(12): 46-51.
[14] GAO Zhenwen, YANG Shuping, XIE Xuexue, SONG Wei. Correlation of Yes-associated protein and the pathological factors of colon cancer [J]. Journal of Shandong University (Health Sciences), 2018, 56(7): 57-64.
[15] HAO Kuiyuan, ZHAO Sheng, ZHANG Yu, CUI Di, JING Yifeng, XIA Shujie, HAN Bangmin. Effect of androgen blockade on autophagy and apoptosis in bladder cancer UM-UC-3 cells [J]. Journal of Shandong University (Health Sciences), 2018, 56(3): 41-47.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!