Evidence map›Paper›PMID 29293402›Full record

ArticleCancer biology & therapy2018

Long noncoding RNA LINP1 acts as an oncogene and promotes chemoresistance in breast cancer.

Yiran Liang, Yaming Li, Xiaojin Song, Ning Zhang, Yuting Sang, Hanwen Zhang, Ying Liu, Bing Chen, Wenjing Zhao, Lijuan Wang and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
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  7. Breast Cancer Chemoresistance: Insights into the Regulatory Role of lncRNA.International journal of molecular sciences · 2023
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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

13 authors at 3 institutions in 1 country.

Yiran Lianga Department of Breast Surgery , Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Yaming Lia Department of Breast Surgery , Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Xiaojin Songa Department of Breast Surgery , Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Ning Zhanga Department of Breast Surgery , Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Yuting Sanga Department of Breast Surgery , Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Hanwen Zhanga Department of Breast Surgery , Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Ying Liua Department of Breast Surgery , Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Bing Chenb Pathology Tissue Bank, Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Wenjing Zhaob Pathology Tissue Bank, Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Lijuan Wangb Pathology Tissue Bank, Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Renbo Guoc Department of Urology , Shandong Cancer Hospital Affiliated to Shandong University , Jinan , Shandong , P.R. China.
Zhigang Yud Department of Breast Surgery , The Second Hospital of Shandong University , Jinan , Shandong , P.R. China.
Qifeng Yanga Department of Breast Surgery , Qilu Hospital, Shandong University , Jinan , Shandong , P.R. China.
Qilu Hospital of Shandong University · CNSecond Hospital of Shandong University · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have shown that long non-coding RNAs (lncRNAs) are involved in a number of biological processes; however, further study is still warranted to comprehensively reveal their functions. In this study, we showed that the lncRNA in non-homologous end joining (NHEJ) pathway 1 (LINP1) was related to breast cancer cell proliferation, metastasis and chemoresistance. Loss- and gain-of function studies were used to assess the role of LINP1 in promoting breast cancer progression. LINP1 knockdown mitigated breast cancer cell growth by inducing G1-phase cell cycle arrest and apoptosis. LINP1 also promoted breast cancer cell metastasis and influenced the expression of epithelial-mesenchymal transition-related markers. We identified p53 as a regulator of LINP1, and LINP1 overexpression could restore the metastatic effects of p53. Furthermore, LINP1 was upregulated in doxorubicin- and 5-fluorouracil-resistant cells and induced chemoresistance. We also observed that LINP1 enrichment played a critical functional role in chemoresistance by inhibiting chemotherapeutics-induced apoptosis. Moreover, LINP1 in tumors was associated with lower overall survival and disease-free survival. In conclusion, LINP1 may serve as a potential oncogene and chemoresistance-related regulator of breast cancer cells, suggesting that LINP1 might be a potent therapeutic target and might reduce chemoresistance in breast cancer.

Indexed as

Antineoplastic AgentsApoptosisBreastBreast NeoplasmsCell Line, TumorCell ProliferationDisease-Free SurvivalDisease ProgressionDoxorubicinDrug Resistance, NeoplasmFemaleFluorouracilFollow-Up StudiesGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansAntineoplastic AgentsDoxorubicinFluorouracilLINP1 non-coding RNA, humanRNA, Long NoncodingRNA, Small Interferingbreast cancerchemoresistanceLINP1oncogene

Identifiers

PMID29293402
PMCPMC5790352
OpenAlexW2782013082

What OpenQuestion holds

Textmetadata
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.