Evidence map›Paper›PMID 41169524›Full record

ArticleJournal of translational internal medicine2025

Lnc5q21.2, a novel long intergenic RNA, sensitizes colorectal cancer cells to ATR inhibitor by activating Wnt pathway.

Meiying Zhang, Cheng Zhu, Aiai Gao, James G Herman, François Fuks, Jianjun Luo, Xiaomo Su, Hengmi Cui, Runsheng Chen, Mingzhou Guo

Abstract read
In one paragraph

Article in Journal of translational internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Epigenetic silencingCancer biology & therapy · 2026
    Article
  2. Article
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.

Meiying ZhangDepartment of Gastroenterology & Hepatology, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
Cheng ZhuDepartment of Gastroenterology & Hepatology, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
Aiai GaoDepartment of Gastroenterology & Hepatology, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
James G HermanThe Hillman Cancer Center, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
François FuksLaboratory of Cancer Epigenetics, Free University of Brussels (U. L.B.), Brussels, Belgium.
Jianjun LuoKey Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Xiaomo SuDepartment of Gastroenterology & Hepatology, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
Hengmi CuiInstitute of Epigenetics and Epigenomics and College of Animal Science and Technology, Yangzhou University, Yangzhou, Jiangsu Province, China.
Runsheng ChenKey Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Mingzhou GuoDepartment of Gastroenterology & Hepatology, the First Medical Center, Chinese PLA General Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-9445-9984

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and objectives: Colorectal cancer (CRC) is still the leading cause of cancer-related death. With the recognizing the importance of long non-coding RNA (LncRNA) in development and cancer, it is urgently to identify new LncRNA and understand the mechanism to develop novel therapeutic strategies. Methods: Nine CRC cell lines, 52,146 and 285 cases of normal colorectal mucosa, adenoma and CRC samples were utilized. Northern blot, rapid amplification of cloned cDNA ends, RNA pulldown, Mass spectrum, RNA immunoprecipitation, CRISPR/Cas9, fluorescence Results: Lnc5q21.2 is identified to be a novel long intergenic non-coding RNA and its full length is 668 nt. Lnc5q21.2 is mainly located in cell nucleus and its expression is regulated by N Conclusions: Lnc5q21.2 is a novel lncRNA. Lnc5q21.2 promotes ATR pathway by activating Wnt signaling via interacting with HOXA10. Lnc5q21.2 sensitizes CRC cells to ATR inhibitor both

Indexed as

ATRcolorectal cancerDNA damage repairLnc5q21.2Wnt signaling

Identifiers

PMID41169524
PMCPMC12569581

What OpenQuestion holds

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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.