Evidence map›Paper›PMID 31384174›Full record

ArticleCancer cell international2019

Inhibition LC3B can increase chemosensitivity of ovarian cancer cells.

Jing Tang, Jiang Zhu, Yuguang Ye, Yu Liu, Yan He, Lei Zhang, Dai Tang, Cong Qiao, Xinxin Feng, Junyi Li and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Subcellular Stress Markers in Epithelial Ovarian Cancer.International journal of molecular sciences · 2025
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  15. [IL-17A/lL-17RA reduces cisplatin sensitivity of ovarian cancer SKOV3 cells by regulating autophagy].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    Article
  16. Review
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

14 authors at 4 institutions in 1 country.

Jing Tang *1Department of Bioinformatics, Southern Medical University, Guangzhou, 510515 China.
Jiang Zhu *3Department of Orthopedics, First Affiliated Hospital of Harbin Medical University, Harbin, 150001 China.
Yuguang Ye *4Department of Gynecology, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, Harbin, 150081 China.
Yu Liu2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Yan He2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Lei Zhang2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Dai Tang2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Cong Qiao2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Xinxin Feng2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Junyi Li2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Yanni Kan2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Xiaobo Li2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Xiaoming Jin2Department of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081 China.
Dan Kong4Department of Gynecology, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, Harbin, 150081 China.
Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CNFirst Affiliated Hospital of Harbin Medical University · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOvarian cancer is often accompanied by the production of ascites, and patients with repeated ascites are associated with chemotherapy resistance. The previous study confirmed that the ovarian cancer patients who developed ascites after chemotherapy had elevated autophagy levels in the ascites and precipitated cells, which was positively correlated with MDR1 expression in the blood of patients.

methodsIn order to explore the correlation between autophagy and chemoresistant, we searched TCGA and GEO database to analyze the correlation between LC3B and MDR1, and identified the targeting miRNA of LC3B. It was verified by dual luciferase that miR-204 can target LC3B. The ovarian cancer cell line and the BALB/c nude mice tumor-bearing model were selected for in vitro and in vivo verification. In vitro studies confirmed that ovarian cancer cells were more sensitive to cisplatin by inhibiting LC3B.

resultsOverexpression of miR-204 reduced the expression of LC3B, Atg7, and MDR1, and promoted apoptosis. In vivo studies have also confirmed that reducing the level of autophagy in ovarian cancer cells increases the sensitivity to cisplatin.

conclusionsIt suggests that miR-204 can be used as a tumor suppressor gene and LC3B expression level can be used as a potential molecular marker to guide the diagnosis and treatment of patients with ovarian cancer.

Indexed as

AutophagyDrug resistanceLC3BmiR-204Ovarian cancer

Identifiers

PMID31384174
PMCPMC6664537
OpenAlexW2965837003

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.