Evidence map›Paper›PMID 38532427›Full record

ArticleMolecular cancer2024

Exosomal long non-coding RNA TRPM2-AS promotes angiogenesis in gallbladder cancer through interacting with PABPC1 to activate NOTCH1 signaling pathway.

Zhiqiang He, Yuhan Zhong, Parbatraj Regmi, Tianrun Lv, Wenjie Ma, Junke Wang, Fei Liu, Siqi Yang, Yanjie Zhong, Rongxing Zhou and 5 more

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
12.3field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Intercellular transfer of LncRNABiochemistry and biophysics reports · 2026
    Article
  5. Review
  6. Macrophage PABPC4-SPP1 Axis Orchestrates Immunosuppression in Colorectal Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. GLS1 Orchestrates Exosome-Mediated Tumor-Endothelial Communication to Facilitate Angiogenesis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Mechanistic insights into the lncRNA-Notch signaling axis in tumors.Frontiers in cell and developmental biology · 2026
    Review
  19. Review
  20. Review
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.

Zhiqiang He *Division of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Yuhan Zhong *Division of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Parbatraj RegmiDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Tianrun LvDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Wenjie MaDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Junke WangDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Fei LiuDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Siqi YangDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Yanjie ZhongDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Rongxing ZhouDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Yanwen JinDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Nansheng ChengDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Yujun ShiKey Laboratory of Transplant Engineering and Immunology, NHFPC, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China.
Haijie HuDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China. hhj1063557621@163.com.
Fuyu LiDivision of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P. R. China. lifuyu@scu.edu.cn.
Sichuan University · CN

Funding

National Natural Science Foundation of China 82203650National Natural Science Foundation of China 82203782Science and Technology Department of Sichuan Province 2022NSFSC0806Sichuan university 2022CDSN-18Sichuan University 2021CDZG-23West China Hospital of Sichuan University 2021HXFH001West China Hospital, Sichuan University ZYJC21046
6 · The paper itself

Abstract

backgroundAbnormal angiogenesis is crucial for gallbladder cancer (GBC) tumor growth and invasion, highlighting the importance of elucidating the mechanisms underlying this process. LncRNA (long non-coding RNA) is widely involved in the malignancy of GBC. However, conclusive evidence confirming the correlation between lncRNAs and angiogenesis in GBC is lacking.

methodsLncRNA sequencing was performed to identify the differentially expressed lncRNAs. RT-qPCR, western blot, FISH, and immunofluorescence were used to measure TRPM2-AS and NOTCH1 signaling pathway expression in vitro. Mouse xenograft and lung metastasis models were used to evaluate the biological function of TRPM2-AS during angiogenesis in vivo. EDU, transwell, and tube formation assays were used to detect the angiogenic ability of HUVECs. RIP, RAP, RNA pull-down, dual-luciferase reporter system, and mass spectrometry were used to confirm the interaction between TRPM2-AS, IGF2BP2, NUMB, and PABPC1.

resultsTRPM2-AS was upregulated in GBC tissues and was closely related to angiogenesis and poor prognosis in patients with GBC. The high expression level and stability of TRPM2-AS benefited from m

conclusionsTRPM2-AS is a novel and promising biomarker for GBC angiogenesis that promotes angiogenesis by facilitating the activation of the NOTCH1 signaling pathway. Targeting TRPM2-AS opens further opportunities for future GBC treatments.

Indexed as

Carcinoma in SituGallbladder NeoplasmsMicroRNAsRNA, Long NoncodingTRPM Cation ChannelsAngiogenesisAnimalsCell Line, TumorCell ProliferationHumansMicePoly(A)-Binding Protein IReceptor, Notch1RNA-Binding ProteinsRNA, MessengerSignal TransductionIGF2BP2 protein, humanMicroRNAsNOTCH1 protein, humanPABPC1 protein, humanPoly(A)-Binding Protein IReceptor, Notch1RNA-Binding ProteinsRNA, Long NoncodingRNA, MessengerTRPM2 protein, humanTRPM2 protein, mouseTRPM Cation ChannelsAngiogenesisExosomeGallbladder cancerIGF2BP2NOTCH1PABPC1TRPM2-AS

Identifiers

PMID38532427
PMCPMC10967197
OpenAlexW4393230240

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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.