Evidence map›Paper›PMID 29367594›Full record

ArticleCell death & disease2018

Long non-coding RNA HOTTIP promotes BCL-2 expression and induces chemoresistance in small cell lung cancer by sponging miR-216a.

Yanqin Sun, Bingshuang Hu, Qiongyao Wang, Minting Ye, Qianqian Qiu, Yuanyuan Zhou, Fanrui Zeng, Xiaomin Zhang, Ying Guo, Linlang Guo

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 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.6field-weighted citation impact, top 2% 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

60 citing papers in PubMed, 108 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

10 authors at 3 institutions in 1 country.

Yanqin SunDepartment of Pathology, Zhujiang Hospital, Southern Medical University, 253 Gongye Road, Guangzhou, 510282, China.
Bingshuang HuDepartment of Pathology, Zhujiang Hospital, Southern Medical University, 253 Gongye Road, Guangzhou, 510282, China.
Qiongyao WangDepartment of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Minting YeDepartment of Pathology, Zhujiang Hospital, Southern Medical University, 253 Gongye Road, Guangzhou, 510282, China.
Qianqian QiuDepartment of Pathology, Zhujiang Hospital, Southern Medical University, 253 Gongye Road, Guangzhou, 510282, China.
Yuanyuan ZhouDepartment of Pathology, Shunde Hospital, Southern Medical University, Foshan, China.
Fanrui ZengDepartment of Pathology, Zhujiang Hospital, Southern Medical University, 253 Gongye Road, Guangzhou, 510282, China.
Xiaomin ZhangDepartment of Dermatology and STD, Changping Hospital, Dongguan, China.
Ying GuoDepartment of Organ Transplantation, Zhujiang Hospital, Southern Medical University, 253 Gongye Road, 510282, Guangzhou, China. guohanjing001@163.com.
Linlang GuoDepartment of Pathology, Zhujiang Hospital, Southern Medical University, 253 Gongye Road, Guangzhou, 510282, China. linlangg@yahoo.com.
Southern Medical University · CNZhujiang Hospital · CNZhongshan People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite progress in treatment of small cell lung cancer (SCLC), its multidrug chemoresistance and poor prognosis still remain. Recently, we globally assessed long non-coding RNAs (lncRNAs) for contributions to SCLC chemoresistance using microarray data, in vitro and in vivo assays. Here we reported that HOTTIP, encoding a lncRNA that is frequently amplified in SCLC, was associated with SCLC cell chemosensitivity, proliferation, and poor prognosis of SCLC patients. Moreover, mechanistic investigations showed that HOTTIP functioned as an oncogene in SCLC progression by binding miR-216a and abrogating its tumor-suppressive function in this setting. On the other hand, HOTTIP increased the expression of anti-apoptotic factor BCL-2, another important target gene of miR-216a, and jointly enhanced chemoresistance of SCLC by regulating BCL-2. Taken together, our study established a role for HOTTIP in SCLC progression and chemoresistance suggest its candidacy as a new diagnostic and prognostic biomarker for clinical management of SCLC.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisBase SequenceCarcinogenesisCell Line, TumorDrug Resistance, NeoplasmFemaleFormaldehydeHomeodomain ProteinsHumansLung NeoplasmsMaleMice, Inbred BALB CMicroRNAsMiddle AgedFormaldehydehomeobox protein HOXA13Homeodomain Proteinslong noncoding RNA HOTTIP, humanMicroRNAsMIRN216 microRNA, humanProto-Oncogene Proteins c-bcl-2RNA, Long Noncoding

Identifiers

PMID29367594
PMCPMC5833383
OpenAlexW2791484822

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.