Atezolizumab and blockade of LncRNA PVT1 attenuate cisplatin resistant ovarian cancer cells progression synergistically via JAK2/STAT3/PD-L1 pathway

被引:25
|
作者
Chen, Ying [1 ,2 ,3 ]
Li, Fangxuan [2 ,3 ,4 ]
Li, Dan [1 ]
Liu, Wenxin [1 ]
Zhang, Lei [1 ,2 ,3 ]
机构
[1] Tianjin Med Univ Canc Inst & Hosp, Dept Gynecol Oncol, Huanhuxi Rd, Tianjin 300060, Peoples R China
[2] Key Lab Canc Prevent & Therapy, Tianjin 300060, Peoples R China
[3] Natl Clin Res Ctr Canc, Tianjin 300060, Peoples R China
[4] Tianjin Med Univ Canc Inst & Hosp, Dept Canc Prevent, Tianjin 300060, Peoples R China
关键词
Long non-coding RNA; Ovarian cancer; PD-L1; PVT1; Resistant; NONCODING RNA; POOR-PROGNOSIS; PD-L1; EXPRESSION; BLADDER-CANCER; GASTRIC-CANCER; DEATH; CARCINOMA; TARGET; AXIS;
D O I
10.1016/j.clim.2021.108728
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To investigate the relationship between lncRNA PVT1(PVT1) level and PD-L1 expression and their functions in cisplatin resistant epithelial ovarian cancer (CREOC). Methods: PVT1 and PD-L1 in ovarian cancer tissues were detected and analyzed. The cells proliferation, apoptosis, invasion abilities and potential mechanism were detected by cell functional experiments and westernblot assay, respectively. Results: The average expressions of PVT1 and PD-L1 in CREOC tissues were significantly higher. The expression of PVT1 is positively associated with PD-L1 in CREOC. Higher expressions of PVT1 and PD-L1 indicated more malignant clinical behavior and shorter PFS and OS. Knockdown of PVT1 inhibited the proliferation and invasion and promote apoptosis for A2780cis cells, which may be related to decrease the expression of PD-L1 via repressing JAK2/STAT3 pathway. Conclusions: The synergistic therapeutic strategy using LncRNA PVT1-targeted therapy and immune checkpoint blockade of PD-L1 warrant study further for ovarian cancer patients with cisplatin resistant recurrence.
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页数:9
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