Evidence map›Paper›PMID 34642309›Full record

ArticleOncogenesis2021

TRPC1 promotes the genesis and progression of colorectal cancer via activating CaM-mediated PI3K/AKT signaling axis.

Yang Sun, Chen Ye, Wen Tian, Wen Ye, Yuan-Yuan Gao, Ying-Da Feng, Hui-Nan Zhang, Guang-Yuan Ma, Shou-Jia Wang, Wei Cao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.7field-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

19 citing papers in PubMed, 33 citations in OpenAlex.

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  17. Roles of calcium signaling in cancer metastasis to bone.Exploration of targeted anti-tumor therapy · 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

11 authors at 2 institutions in 1 country.

Yang Sun *Department of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.ORCID http://orcid.org/0000-0002-3456-4221
Chen Ye *Department of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.ORCID http://orcid.org/0000-0002-8493-944X
Wen Tian *Department of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.ORCID http://orcid.org/0000-0001-5074-1059
Wen YeDepartment of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.ORCID http://orcid.org/0000-0002-0171-7439
Yuan-Yuan GaoDepartment of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.ORCID http://orcid.org/0000-0002-6051-9838
Ying-Da FengDepartment of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.ORCID http://orcid.org/0000-0001-8642-4477
Hui-Nan ZhangDepartment of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.ORCID http://orcid.org/0000-0002-1440-2049
Guang-Yuan MaDepartment of Pharmacy, School of Chemistry & Pharmacy, Northwest A&F University, Yangling, Shaanxi, 712100, China.ORCID http://orcid.org/0000-0001-9257-7891
Shou-Jia WangDepartment of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.ORCID http://orcid.org/0000-0001-5797-5608
Wei CaoKey Laboratory of Gastrointestinal Pharmacology of Chinese Materia Medica of the State Administration of Traditional Chinese Medicine, Xi'an, Shaanxi, 710032, China. caowei@nwafu.edu.cn.ORCID http://orcid.org/0000-0003-3863-137X
Xiao-Qiang LiDepartment of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, 710032, China. xxqqli@fmmu.edu.cn.ORCID http://orcid.org/0000-0003-2463-8298
State Administration of Traditional Chinese Medicine of the People's Republic of China · CNNorthwest A&F University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81770432National Natural Science Foundation of China (National Science Foundation of China) 81970245Northwest A and F University (Northwest A & F University) 2452017335Shaanxi Provincial Science and Technology Department (Science and Technology Department, Shaanxi Province) 2019PT-23Shaanxi Provincial Science and Technology Department (Science and Technology Department, Shaanxi Province) 2019ZDLSF04-03-01
6 · The paper itself

Abstract

Transient receptor potential canonical (TRPC) channels are the most prominent nonselective cation channels involved in various diseases. However, the function, clinical significance, and molecular mechanism of TRPCs in colorectal cancer (CRC) progression remain unclear. In this study, we identified that TRPC1 was the major variant gene of the TRPC family in CRC patients. TRPC1 was upregulated in CRC tissues compared with adjacent normal tissues and high expression of TRPC1 was associated with more aggressive tumor progression and poor overall survival. TRPC1 knockdown inhibited cell proliferation, cell-cycle progression, invasion, and migration in vitro, as well as tumor growth in vivo; whereas TRPC1 overexpression promoted colorectal tumor growth and metastasis in vitro and in vivo. In addition, colorectal tumorigenesis was significantly attenuated in Trpc1

Identifiers

PMID34642309
PMCPMC8511127
OpenAlexW3206446926

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.