Long Noncoding RNA Cancer Susceptibility Candidate 9 Promotes Chemotherapy Resistance of Non-Small Cell Lung Cancer

被引:0
|
作者
Chen, Ding Zhu [1 ]
Zhang, Yi [1 ]
Lin, Yong [1 ]
Huang, Yu Zhen [2 ]
Zhang, Zhi Jian [3 ]
Zhou, Ji Guang [4 ]
Tian, Qing Yong [1 ]
Chen, Jun Biao [1 ]
机构
[1] Fujian Med Univ, Zhangzhou Hosp, Dept Cardiac & Thorac, 59 Shenglixi Rd, Zhangzhou 363000, Fujian, Peoples R China
[2] Fujian Med Univ, Zhangzhou Hosp, Dept Pathol, 59 Shenglixi Rd, Zhangzhou 363000, Fujian, Peoples R China
[3] Fujian Med Univ, Zhangzhou Hosp, Dept Clin Lab, 59 Shenglixi Rd, Zhangzhou 363000, Fujian, Peoples R China
[4] Fujian Med Univ, Zhangzhou Hosp, Dept Informat Ctr, 59 Shenglixi Rd, Zhangzhou 363000, Fujian, Peoples R China
关键词
Non-small cell lung cancer; gefitinib; microRNA-382-5p; rapamycin; METASTASIS; EXPRESSION;
D O I
10.36468/pharmaceutical-sciences.spl.307
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To investigate the molecular mechanism of long noncoding RNA cancer susceptibility candidate 9 involved in gefitinib resistance in non-small cell lung cancer cells by regulating microRNA-382-5p/ phosphoinositidedependent protein kinase-1/mammalian target of rapamycin complex 2 signal axis. 10 cases of serum before treatment and 10 cases of drug resistant serum after gefitinib treatment were collected from December 2019 to December 2020. The expression levels in non-small cell lung cancer tissues or cell lines were detected by real-time quantitative reverse transcription polymerase chain reaction. Cell counting kit 8, transwell and cell flow cytometry were used to detect the sensitivity of non-small cell lung cancer cells to gifetinib. Double luciferase reporter assay was used to verify the targeting relationship and the regulatory relationship was detected by western blotting and real-time quantitative reverse transcription polymerase chain reaction. Cancer susceptibility candidate 9 was highly expressed in non-small cell lung cancer tissues and drug-resistant HCC827/G cells. Overexpression of cancer susceptibility candidate 9 can significantly promote the proliferation, invasion and inhibit apoptosis of HCC827/G cells. At the same time, dual luciferase reporter assay confirmed that cancer susceptibility candidate 9 could negatively regulate the expression of microRNA-382-5p and microRNA-185-5p could bind to the 3'UTR of phosphoinositidedependent protein kinase-1 and mammalian target of rapamycin complex 2 and negatively regulate the expression of phosphoinositide-dependent protein kinase-1 and mammalian target of rapamycin complex 2. Further experiments showed that cancer susceptibility candidate 9 could up regulate the drug resistance of HCC827/G cells to gefitinib by down regulating the inhibition of microRNA-382-5p on phosphoinositide-dependent protein kinase-1 and mammalian target of rapamycin complex 2, thereby promoting the proliferation, invasion and inhibiting apoptosis of HCC827/G cells. Cancer susceptibility candidate 9 induces gefitinib resistance in non-small cell lung cancer cells by regulating microRNA-3825p/phosphoinositide-dependent protein kinase-1/mammalian target of rapamycin complex 2 signal axis.
引用
收藏
页码:144 / 152
页数:9
相关论文
共 50 条
  • [31] Long noncoding RNA TCF7 promotes invasiveness and self-renewal of human non-small cell lung cancer cells
    Wu, Jinhui
    Wang, Dongshuang
    HUMAN CELL, 2017, 30 (01): : 23 - 29
  • [32] RETRACTED: Long noncoding RNA OR3A4 promotes cisplatin resistance of non-small cell lung cancer by upregulating CDK1 (Retracted Article)
    Shang, J.
    Xu, Y-D
    Zhang, Y-Y
    Li, M.
    EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, 2019, 23 (10) : 4220 - 4225
  • [33] Long noncoding RNA CRNDE promotes non-small cell lung cancer progression via sponging microRNA-338-3p
    Jing, Hongyu
    Xia, Huan
    Qian, Ming
    Lv, Xiaohong
    BIOMEDICINE & PHARMACOTHERAPY, 2019, 110 : 825 - 833
  • [34] The Roles of microRNAs in Regulating Chemotherapy Resistance of Non-Small Cell Lung Cancer
    Wei, Xiaoxuan
    Shen, Xiaoyan
    Ren, Yanchen
    Hu, Weidong
    CURRENT PHARMACEUTICAL DESIGN, 2017, 23 (39) : 5983 - 5988
  • [35] VGF is functionally responsible for chemotherapy resistance in non-small cell lung cancer
    Nogami, Wataru
    Tona, Yumi
    Tofukuji, Soichi
    Ishioka, Yoshino
    Matsumoto, Mitsunobu
    Yamada, Hajime
    Kuwabara, Kenji
    Tanaka, Hidekazu
    Adachi, Shigeki
    Yamamoto, Yoko
    Kanzaki, Ryu
    Funaki, Soichiro
    Shintani, Yasushi
    Okumura, Meinoshin
    Nomura, Taisei
    CANCER RESEARCH, 2019, 79 (13)
  • [36] AN INDUCIBLE SYSTEM TO STUDY CHEMOTHERAPY RESISTANCE IN NON-SMALL CELL LUNG CANCER
    Marti, T. M.
    Albisser, M. L.
    Kotov, I. N.
    Shi, Y.
    Felley-Bosco, E.
    Stahel, R. A.
    JOURNAL OF THORACIC ONCOLOGY, 2012, 7 (06) : S42 - S42
  • [37] Tamoxifen as a potential inhibitor of the chemotherapy resistance in non-small cell lung cancer
    Bogush, T. A.
    Dudko, E. A.
    Bogush, E. A.
    Tikchomirov, M. V.
    Ramanayskaite, R. J.
    Laktionov, K. K.
    Polotsky, B. E.
    Davydov, M. I.
    EJC SUPPLEMENTS, 2010, 8 (05): : 64 - 64
  • [38] Maintenance Chemotherapy in Non-Small Cell Lung Cancer
    Eaton, Keith D.
    Martins, Renato G.
    JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2010, 8 (07): : 815 - 821
  • [39] CHEMOTHERAPY OF NON-SMALL CELL LUNG-CANCER
    MITROU, PS
    KLIPPSTEIN, T
    LAUTENSCHLAGER, G
    ATEMWEGS-UND LUNGENKRANKHEITEN, 1986, 12 (11) : 544 - 549
  • [40] Neoadjuvant chemotherapy in non-small cell lung cancer
    Niklinski, J
    8TH CENTRAL EUROPEAN LUNG CANCER CONFERENCE, 2002, : 217 - 223