Evidence map›Paper›PMID 28765565›Full record

ArticleScientific reports2017

Telomerase reverse transcriptase promotes chemoresistance by suppressing cisplatin-dependent apoptosis in osteosarcoma cells.

Zhengpei Zhang, Ling Yu, Guo Dai, Kezhou Xia, Gaiwei Liu, Qi Song, Chunjie Tao, Tian Gao, Weichun Guo

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. bioRxiv : the preprint server for biology · 2026
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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

9 authors at 3 institutions in 1 country.

Zhengpei ZhangDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Ling YuDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, Hubei, China. scaling@whu.edu.cn.
Guo DaiDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Kezhou XiaDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Gaiwei LiuDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Qi SongDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Chunjie TaoDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Tian GaoKey Laboratory of Carcinogenesis and Translational Research, Ministry of Education, Department of Orthopedic Oncology, Peking University Cancer Hospital& Institute, Beijing, China.
Weichun GuoDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, Hubei, China. guoweichun@aliyun.com.
Renmin Hospital of Wuhan University · CNWuhan University · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cisplatin is one of the most efficacious antimitotic drugs used in the treatment of a range of malignant tumors. However, treatment failures are common due to the development of chemoresistance. In addition to its telomere maintenance function, telomerase plays a pro-survival role, inducing decreased apoptosis and increased resistance against DNA damage. Elucidation of the molecular mechanisms underlying this effect is critical to improve treatment outcomes. Previously, our group showed higher telomerase reverse transcriptase(TERT) expression in cisplatin resistant osteosarcoma cells. In this study, confocal fluorescence microscopy experiments revealed that TERT translocates from the nucleus to mitochondria in cisplatin treated osteosarcoma cells. We observed decreased apoptosis rate and improved mitochondrial function in TERT-overexpressing cells following cisplatin treatment. Based on these results, we further established that TERT inhibits cisplatin-induced apoptosis independently of telomerase reverse transcriptase activity. Moreover, TERT suppressed cisplatin-induced apoptosis and improved mitochondrial function via alleviating intracellular ROS in osteosarcoma cells. Our finding that TERT shuttles from the nucleus to the mitochondrion in response to cisplatin treatment and inhibits cisplatin-induced apoptosis in osteosarcoma cells may be especially important to overcome drug resistance.

Indexed as

ApoptosisDrug Resistance, NeoplasmAntineoplastic AgentsCell Line, TumorCisplatinHumansMicroscopy, ConfocalMicroscopy, FluorescenceOsteosarcomaProtein TransportTelomeraseAntineoplastic AgentsCisplatinTelomerase

Identifiers

PMID28765565
PMCPMC5539325
OpenAlexW2738742181

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.