Evidence map›Paper›PMID 34262130›Full record

ArticleOncogene2021

CRIP1 cooperates with BRCA2 to drive the nuclear enrichment of RAD51 and to facilitate homologous repair upon DNA damage induced by chemotherapy.

Huiying Sun, Rui Zhou, Yannan Zheng, Zhaowei Wen, Dingling Zhang, Dongqiang Zeng, Jianhua Wu, Zhenhua Huang, Xiaoxiang Rong, Na Huang and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 50 citations in OpenAlex.

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  19. Comprehensive Analysis ofFrontiers in genetics · 2022
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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

15 authors at 1 institution in 1 country.

Huiying Sun *Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Rui Zhou *Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China. dr.zhourui@qq.com.ORCID http://orcid.org/0000-0002-8250-9446
Yannan ZhengDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Zhaowei WenDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Dingling ZhangDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Dongqiang ZengDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.ORCID http://orcid.org/0000-0001-9724-8325
Jianhua WuDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Zhenhua HuangDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Xiaoxiang RongDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Na HuangDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Li SunDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Jianping BinDepartment of Cardiology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Yulin LiaoDepartment of Cardiology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.ORCID http://orcid.org/0000-0001-5961-390X
Min ShiDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China.
Wangjun LiaoDepartment of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, PR China. nfyyliaowj@163.com.ORCID http://orcid.org/0000-0002-1364-8442
Nanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homologous recombination (HR) repair is an important determinant of chemosensitivity. However, the mechanisms underlying HR regulation remain largely unknown. Cysteine-rich intestinal protein 1 (CRIP1) is a member of the LIM/double-zinc finger protein family and is overexpressed and associated with prognosis in several tumor types. However, to date, the functional role of CRIP1 in cancer biology is poorly understood. Here we found that CRIP1 downregulation causes HR repair deficiency with concomitant increase in cell sensitivity to cisplatin, epirubicin, and the poly ADP-ribose polymerase (PARP) inhibitor olaparib in gastric cancer cells. Mechanistically, upon DNA damage, CRIP1 is deubiquitinated and upregulated by activated AKT signaling. CRIP1, in turn, promotes nuclear enrichment of RAD51, which is a prerequisite step for HR commencement, by stabilizing BRCA2 to counteract FBXO5-targeted RAD51 degradation and by binding to the core domain of RAD51 (RAD51

Indexed as

BRCA2 ProteinDNA DamageLIM Domain ProteinsRad51 RecombinaseRecombinational DNA RepairStomach NeoplasmsCarrier ProteinsCell Line, TumorCell NucleusCisplatinEpirubicinHumansPhthalazinesPiperazinesBRCA2 ProteinBRCA2 protein, humanCarrier ProteinsCisplatinCRIP1 protein, humanEpirubicinLIM Domain ProteinsolaparibPhthalazinesPiperazinesRAD51 protein, humanRad51 Recombinase

Identifiers

PMID34262130
PMCPMC8390368
OpenAlexW3182847262

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.