Evidence map›Paper›PMID 30643427›Full record

ArticleOncoTargets and therapy2019

Contribution of FPR and TLR9 to hypoxia-induced chemoresistance of ovarian cancer cells.

Yongqing Cai, Jian Huang, Haiyan Xing, Bin Li, Ling Li, Xianfeng Wang, Dan Peng, Jianhong Chen

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Yongqing CaiDepartment of Pharmacy, Daping Hospital and Research Institute of Surgery, Army Medical University, Chongqing 400042, China, chenjh-110@263.net.
Jian HuangDepartment of High Altitude Biology and Pathology, High Altitude Military Medical College, Army Medical University, Chongqing 400042, China.
Haiyan XingDepartment of Pharmacy, Daping Hospital and Research Institute of Surgery, Army Medical University, Chongqing 400042, China, chenjh-110@263.net.
Bin LiDepartment of Pharmacy, Daping Hospital and Research Institute of Surgery, Army Medical University, Chongqing 400042, China, chenjh-110@263.net.
Ling LiDepartment of Pharmacy, Daping Hospital and Research Institute of Surgery, Army Medical University, Chongqing 400042, China, chenjh-110@263.net.
Xianfeng WangDepartment of Pharmacy, Daping Hospital and Research Institute of Surgery, Army Medical University, Chongqing 400042, China, chenjh-110@263.net.
Dan PengDepartment of Pharmacy, Daping Hospital and Research Institute of Surgery, Army Medical University, Chongqing 400042, China, chenjh-110@263.net.
Jianhong ChenDepartment of Pharmacy, Daping Hospital and Research Institute of Surgery, Army Medical University, Chongqing 400042, China, chenjh-110@263.net.
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background/purposeThe aim of this study was to investigate the role and mechanisms of the formyl peptide receptor (FPR) and the toll-like receptor 9 (TLR9) in hypoxia-induced chemoresistance of human ovarian cancer cells. MATERIALS AND

methodsSKOV3 cells were exposed to hypoxia for 24 hours, the supernatant was collected to stimulate normoxia-cultured SKOV3, and the inhibition rate of cell growth was detected with CCK8 test. The agonist of TLR9 CpG ODN and the agonist of FPR fMLF were applied to investigate the chemosensitivity of SKOV3 cells to cisplatin. The cells were also treated with FPR antagonist t-Boc or TLR9 antagonist CQ. Western blot was applied to detect protein levels of FPR, TLR9, MRP, P-gp, p53 and Beclin-1. Immunofluorescence staining was applied to observe the distribution of TLR9 in SKOV3 cells.

resultsHypoxia exposure reduced the inhibition rate of cisplatin on SKOV3 cells. WB showed that FPR and TLR9 were expressed in human ovarian cancer tissues and SKOV3 cells, and the levels were increased with longer hypoxia time. After SKOV3 was stimulated with fMLF or ODN2006, cisplatin-induced inhibition rate was significantly decreased. tBoc and CQ significantly attenuated hypoxia supernatant-induced chemoresistance of SKOV3 cells. Hypoxia supernatants significantly increased MRP, P-gp, p53 and Beclin-1 proteins in SKOV3 cells, which were significantly reduced by tBoc.

conclusionHypoxia upregulates the expression of FPR and TLR9, and promotes the release of ligands for both receptors in human ovarian cancer cell line. FPR and TLR9 may be noval targets for chemosensitizing to ovarian cancer cells.

Indexed as

Beclin-1chemoresistanceFPRHICRhuman ovarian cancerhypoxiaMRPTLR9

Identifiers

PMID30643427
PMCPMC6314315
OpenAlexW2907073776

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.