Evidence map›Paper›PMID 29549251›Full record

ArticleCell death & disease2018

Increased autophagy in EOC re-ascites cells can inhibit cell death and promote drug resistance.

Yu Liu, Jing Tang, Duanyang Liu, Lei Zhang, Yan He, Jing Li, Lei Gao, Dai Tang, Xiaoming Jin, Dan Kong

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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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

10 authors at 2 institutions in 1 country.

Yu LiuDepartment of Pathology, Harbin Medical University, Harbin, China.
Jing TangDepartment of Pathology, Harbin Medical University, Harbin, China.
Duanyang LiuDepartment of Pathology, Harbin Medical University, Harbin, China.
Lei ZhangDepartment of Pathology, Harbin Medical University, Harbin, China.
Yan HeDepartment of Pathology, Harbin Medical University, Harbin, China.
Jing LiElectron Microscopic Center, Harbin Medical University, Harbin, China.
Lei GaoElectron Microscopic Center, Harbin Medical University, Harbin, China.
Dai TangDepartment of Pathology, Harbin Medical University, Harbin, China.
Xiaoming JinDepartment of Pathology, Harbin Medical University, Harbin, China. jinxm55@163.com.
Dan KongDepartment of Gynecology, Tumor Hospital of Harbin Medical University, Harbin, China. 15395030@qq.com.
Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the major and preferred treatment for ovarian cancer ascites, chemotherapy can reduce or inhibit recurrent ascites (hereafter re-ascites); however, some patients still experience re-ascites. Therefore, this study investigated cases in which epithelial ovarian cancer (EOC) patients experienced re-ascites. In re-ascites cases, CA125, MDR1, LC-3, and Beclin-1 were highly expressed. In addition, CASP-9 and c-CASP-3 expression levels were decreased, and serum CA125 levels (highest 4348 U/ml) were increased compared to chemosensitive cases. The results suggest that high expression levels of Beclin-1 and LC-3, thus increasing the level of autophagy and inhibiting apoptosis in the no-chemotherapy group. In the chemosensitive group, survivin expression was decreased and CASP-9 expression was increased, which led to c-CASP-3 activation and increased tumor cell apoptosis. The results of the cell lines confirm that inhibition of autophagy can increase the sensitivity of ovarian cancer cells to CDDP and promote CDDP-induced cell death. Re-ascites, which appears after chemotherapy, may be associated with drug resistance. In addition, increased autophagy may protect tumor cells from chemotherapeutic drugs, thus inhibiting tumor cell death.

Indexed as

ApoptosisAutophagyDrug Resistance, NeoplasmAntineoplastic AgentsAscitesBeclin-1CA-125 AntigenCarcinoma, Ovarian EpithelialCaspase 3Caspase 9Cell Line, TumorCisplatinFemaleHumansMicrotubule-Associated ProteinsProto-Oncogene Proteins c-aktAntineoplastic AgentsBeclin-1CA-125 AntigenCaspase 3Caspase 9CisplatinMAP1LC3A protein, humanMicrotubule-Associated ProteinsProto-Oncogene Proteins c-akt

Identifiers

PMID29549251
PMCPMC5856849
OpenAlexW2794069050

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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.