Evidence map›Paper›PMID 39005692›Full record

ArticleAmerican journal of cancer research2024

The long non-coding RNA CCAT1 promotes erlotinib resistance in cholangiocarcinoma by inducing epithelial-mesenchymal transition via the miR-181a-5p/ROCK2 axis.

Wei Zhou, Xingquan Li, Bolin Zhang, Hong Peng, Chunyang Quan, Xin Xiao, Man Luo, Yanxiao Huang, Debin Xu, Kai Huang and 2 more

Abstract read
In one paragraph

Article in American journal of cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
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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

12 authors.

Wei ZhouDepartment of Abdominal Surgery, Jiangxi Cancer Hospital Nanchang 330029, Jiangxi, China.
Xingquan LiDepartment of General Surgery, Jiangxi Cancer Hospital, Jiangxi Medical College, Nanchang University Nanchang 330029, Jiangxi, China.
Bolin ZhangDepartment of General Surgery, Jiangxi Cancer Hospital, Jiangxi Medical College, Nanchang University Nanchang 330029, Jiangxi, China.
Hong PengDepartment of Colorectal Surgery, 908th Hospital of Chinese People's Liberation Army Joint Nanchang 330029, Jiangxi, China.
Chunyang QuanDepartment of General Surgery, Jiangxi Cancer Hospital, Jiangxi Medical College, Nanchang University Nanchang 330029, Jiangxi, China.
Xin XiaoDepartment of General Surgery, Jiangxi Cancer Hospital, Jiangxi Medical College, Nanchang University Nanchang 330029, Jiangxi, China.
Man LuoDepartment of General Surgery, Jiangxi Cancer Hospital, Jiangxi Medical College, Nanchang University Nanchang 330029, Jiangxi, China.
Yanxiao HuangDepartment of General Surgery, Jiangxi Cancer Hospital, Jiangxi Medical College, Nanchang University Nanchang 330029, Jiangxi, China.
Debin XuDepartment of General Surgery, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University Nanchang 330006, Jiangxi, China.
Kai HuangDepartment of Abdominal Surgery, Jiangxi Cancer Hospital Nanchang 330029, Jiangxi, China.
Qifang JinDepartment of Ophthalmology, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University Nanchang 330006, Jiangxi, China.
Shan LuOncology Teaching and Research Office, The Second Affiliated Hospital of Nanchang Medical College Nanchang 330029, Jiangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholangiocarcinoma (CCA) is a common malignancy of the digestive system, and its treatment is greatly challenged by rising chemoresistance. Long non-coding RNAs (lncRNAs) have been shown to play critical roles in the development of drug resistance in tumors. However, the role of the lncRNA CCAT1 in erlotinib resistance in CCA remains unclear. In this investigation, we identified CCAT1 as a pivotal factor contributing to erlotinib resistance in CCA. Furthermore, we uncovered that lncRNA CCAT1 modulated epithelial-mesenchymal transition (EMT) through Rho-associated coiled-coil-forming protein kinase 2 (ROCK2), thereby conferring erlotinib resistance upon CCA cells. Mechanistically, we demonstrated that miR-181a-5p interacted with CCAT1 to modulate the expression of ROCK2. Collectively, these findings shed light on the significant role of CCAT1 in the development of erlotinib resistance in CCA. The functional suppression of CCAT1 holds promise in enhancing the sensitivity to erlotinib by reversing EMT through the miR-181a-5p/ROCK2 signaling pathway. These findings provide valuable insights into the mechanisms underlying erlotinib resistance in CCA and the potential strategies for its treatment.

Indexed as

CholangiocarcinomaEMTerlotinib resistancelncRNA CCAT1ROCK2

Identifiers

PMID39005692
PMCPMC11236789

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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.