炎症细胞因子在卵巢上皮癌化疗耐药中的作用

国际肿瘤学杂志››2020,Vol. 47››Issue (4): 249-251.doi:10.3760/cma.j.cn371439-20191010-00012

炎症细胞因子在卵巢上皮癌化疗耐药中的作用

杨怡婷, 程忠平()

南京医科大学上海第十人民医院临床医学院,上海 200072

收稿日期:2019-10-10修回日期:2020-03-27出版日期:2020-04-08发布日期:2020-05-26
通讯作者:程忠平 E-mail:mdcheng@tongji.edu.cn
基金资助:
国家自然科学基金(81874104)

The role of inflammatory cytokines in chemoresistance of epithelial ovarian cancer

Yang Yiting, Cheng Zhongping()

School of Clinical Medicine, Shanghai the Tenth People's Hospital, Nanjing Medical University,Shanghai 200072, China

Received:2019-10-10Revised:2020-03-27Online:2020-04-08Published:2020-05-26
Contact:Cheng Zhongping E-mail:mdcheng@tongji.edu.cn
Supported by:
National Natural Science Foundation of China(81874104)

摘要/Abstract

摘要：

卵巢癌是女性常见的致命性恶性肿瘤,最常见的病理类型是起源于卵巢或输卵管上皮的卵巢上皮癌(EOC),约占85%~90%。EOC患者的标准治疗方法是肿瘤细胞减灭术,术后进行铂类/紫杉醇化疗,细胞的化疗耐药已成为EOC患者复发并走向死亡的重要原因。目前已有许多学者认为卵巢癌的肿瘤环境富含广谱的肿瘤促炎细胞因子和趋化因子。炎症能使上皮细胞分裂分化增加,正常的上皮组织长期暴露于炎性环境会逐渐向恶性转化,炎性肿瘤微环境促进转变的恶性肿瘤细胞侵袭、转移,最终发生耐药。

关键词:卵巢肿瘤,活性氧,白细胞介素6,白细胞介素8,溶血磷脂素类

Abstract:

Ovarian cancer is a common fatal malignant tumor in women. The most common pathological type is epithelial ovarian cancer (EOC) originating from the ovary or fallopian tube epithelium, accounting for 85%-90%. The standard treatment for EOC is tumor cytoreductive surgery. Postoperative platinum/paclitaxel chemotherapy, cell chemoresistance has become an important cause of recurrence and death in EOC patients. At present, many scholars believe that the tumor environment of ovarian cancer is rich in a broad spectrum of tumor pro-inflammatory cytokines and chemokines. Inflammation can increase the division and differentiation of epithelial cells. The long-term exposure of normal epithelial tissues to the inflammatory environment will gradually turn to malignant transformation. The inflammatory tumor microenvironment promotes the invasion and metastasis of transformed malignant tumor cells, and eventually develops drug resistance.

Key words:Ovarian neoplasms,Reactive oxygen species,Interleukin-6,Interleukin-8,Lysophospholipids

杨怡婷, 程忠平. 炎症细胞因子在卵巢上皮癌化疗耐药中的作用[J]. 国际肿瘤学杂志, 2020, 47(4): 249-251.

Yang Yiting, Cheng Zhongping. The role of inflammatory cytokines in chemoresistance of epithelial ovarian cancer[J]. Journal of International Oncology, 2020, 47(4): 249-251.

参考文献24

[1]	Savant SS, Sriramkumar S, O'Hagan HM. The Role of inflammation and inflammatory mediators in the development, progression, metastasis, and chemoresistance of epithelial ovarian cancer[J]. Cancers (Basel), 2018, 10(8). pii: E251. DOI: 10.3390/cancers10080251.
[2]	Xuan Y, Wang YN . Hypoxia/IL-1α axis promotes gastric cancer progression and drug resistance[J]. J Dig Dis, 2017,18(9):511-520. DOI: 10.1111/1751-2980.12496. doi:10.1111/cdd.2017.18.issue-9
[3]	Yu Y, Zhang Q, Ma C , et al. Mesenchymal stem cells recruited by castration-induced inflammation activation accelerate prostate cancer hormone resistance via chemokine ligand 5 secretion[J]. Stem Cell Res Ther, 2018,9(1):242. DOI: 10.1186/s13287-018-0989-8. doi:10.1186/s13287-018-0989-8
[4]	李研 . 白藜芦醇对卵巢癌细胞顺铂化疗的增敏作用[J]. 国际肿瘤学杂志, 2018,45(1):5-9. DOI: 10.3760/cma.j.issn.1673-422X.2018.01.002.
[5]	Vaidyanathan A, Sawers L, Gannon AL , et al. ABCB1 (MDR1) induction defines a common resistance mechanism in paclitaxel- and olaparib-resistant ovarian cancer cells[J]. Br J Cancer, 2016,115(4):431-441. DOI: 10.1038/bjc.2016.203. doi:10.1038/bjc.2016.203
[6]	Kenda Suster N, Smrkolj S, Virant-Klun I . Putative stem cells and epithelial-mesenchymal transition revealed in sections of ovarian tumor in patients with serous ovarian carcinoma using immunohistochemistry for vimentin and pluripotency-related markers[J]. J Ovarian Res, 2017,10(1):11. DOI: 10.1186/s13048-017-0306-7. doi:10.1186/s13048-017-0306-7
[7]	Ricci F, Carrassa L, Christodoulou MS , et al. A high-throughput screening of a chemical compound library in ovarian cancer stem cells[J]. Comb Chem High Throughput Screen, 2018,21(1):50-56. DOI: 10.2174/1386207321666180124093406. doi:10.2174/1386207321666180124093406
[8]	Cohen S, Mehrabi S, Yao X , et al. Reactive oxygen species and serous epithelial ovarian adenocarcinoma[J]. Cancer Res J (N Y N Y), 2016,4(6):106-114. DOI: 10.11648/j.crj.20160406.13.
[9]	Nunes SC, Serpa J. Glutathione in ovarian cancer: a double-edged sword[J]. Int J Mol Sci, 2018, 19(7). pii: E1882. DOI: 10.3390/ijms19071882.
[10]	Bansal A, Simon MC . Glutathione metabolism in cancer progression and treatment resistance[J]. J Cell Biol, 2018,217(7):2291-2298. DOI: 10.1083/jcb.201804161. doi:10.1083/jcb.201804161
[11]	Browning L, Patel MR, Horvath EB , et al. IL-6 and ovarian cancer: inflammatory cytokines in promotion of metastasis[J]. Cancer Manag Res, 2018,10:6685-6693. DOI: 10.2147/CMAR.S179189. doi:10.2147/CMAR
[12]	Wang L, Zhang F, Cui JY , et al. CAFs enhance paclitaxel resistance by inducing EMT through the IL6/JAK2/STAT3 pathway[J]. Oncol Rep, 2018,39(5):2081-2090. DOI: 10.3892/or.2018.6311.
[13]	Pasquier J, Gosset M, Geyl C , et al. CCL2/CCL5 secreted by the stroma induce IL-6/PYK2 dependent chemoresistance in ovarian cancer[J]. Mol Cancer, 2018,17(1):47. DOI: 10.1186/s12943-018-0787-z. doi:10.1186/s12943-018-0787-z
[14]	Devapatla B, Sharma A, Woo S . CXCR2 inhibition combined with sorafenib improved antitumor and antiangiogenic response in preclinical models of ovarian cancer[J]. PLoS One, 2015,10(9):e0139237. DOI: 10.1371/journal.pone.0139237. doi:10.1371/journal.pone.0139237
[15]	Wen J, Zhao Z, Huang L , et al. IL-8 promotes cell migration through regulating EMT by activating the Wnt/beta-catenin pathway in ovarian cancer[J]. J Cell Mol Med, 2020,24(2):1588-1598. DOI: 10.1111/jcmm.14848. doi:10.1111/jcmm.v24.2
[16]	Li L, Yu J, Duan Z , et al. The effect of NFATc1 on vascular generation and the possible underlying mechanism in epithelial ovarian carcinoma[J]. Int J Oncol, 2016,48(4):1457-1466. DOI: 10.3892/ijo.2016.3355. doi:10.3892/ijo.2016.3355
[17]	Cheng M, Cai W, Huang W , et al. Histone deacetylase 6 regulated expression of IL-8 is involved in the doxorubicin (Dox) resistance of osteosarcoma cells via modulating ABCB1 transcription[J]. Eur J Pharmacol, 2018,840:1-8. DOI: 10.1016/j.ejphar.2018.09.032. doi:10.1016/j.ejphar.2018.09.032
[18]	Stronach EA, Cunnea P, Turner C , et al. The role of interleukin-8 (IL-8) and IL-8 receptors in platinum response in high grade serous ovarian carcinoma[J]. Oncotarget, 2015,6(31):31593-31603. DOI: 10.18632/oncotarget.3415. doi:10.18632/oncotarget.v6i31
[19]	Yin J, Zeng F, Wu N , et al. Interleukin-8 promotes human ovarian cancer cell migration by epithelial-mesenchymal transition induction in vitro[J]. Clin Transl Oncol, 2015,17(5):365-370. DOI: 10.1007/s12094-014-1240-4. doi:10.1007/s12094-014-1240-4
[20]	Suckau O, Gross I, Schrötter S , et al. LPA₁, LPA₂, LPA₄, and LPA₆receptor expression during mouse brain development[J]. Dev Dyn, 2019,248(5):375-395. DOI: 10.1002/dvdy.23. doi:10.1002/dvdy.v248.5
[21]	Xu Y. Lysophospholipid signaling in the epithelial ovarian cancer tumor microenvironment[J]. Cancers (Basel), 2018, 10(7). pii: E227. DOI: 10.3390/cancers10070227.
[22]	Ray U, Roy SS, Chowdhury SR . Lysophosphatidic acid promotes epithelial to mesenchymal transition in ovarian cancer cells by repressing SIRT1[J]. Cell Physiol Biochem, 2017,41(2):795-805. DOI: 10.1159/000458744. doi:10.1159/000458744
[23]	Rogers LC, Davis RR, Said N , et al. Blocking LPA-dependent signaling increases ovarian cancer cell death in response to chemotherapy[J]. Redox Biol, 2018,15:380-386. DOI: 10.1016/j.redox.2018.01.002. doi:10.1016/j.redox.2018.01.002
[24]	Seo EJ, Kwon YW, Jang IH , et al. Autotaxin regulates maintenance of ovarian cancer stem cells through lysophosphatidic acid-mediated autocrine mechanism[J]. Stem Cells, 2016,34(3):551-564. DOI: 10.1002/stem.2279. doi:10.1002/stem.2279