Evidence map›Paper›PMID 36817036›Full record

ArticleOncology letters2023

TRPC7 facilitates cell growth and migration by regulating intracellular Ca

Jui-Lin Liang, Ming-Hsien Tsai, Yi-Chun Hsieh, Huei-Syuan Liu, Shao-Wei Chen, Yung-Yun Huang, Li-Ching Lin, Tsung-Fu Tsai, Yun-Fang Liang, Wen-Li Hsu

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Role of TRP Channels in Metabolism-Related Diseases.International journal of molecular sciences · 2024
    Review
  5. Review
  6. 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

10 authors at 6 institutions in 1 country.

Jui-Lin LiangInstitute of Clinical Medicine, National Cheng Kung University College of Medicine, Tainan 701401, Taiwan, R.O.C.
Ming-Hsien TsaiDepartment of Child Care, National Pingtung University of Science and Technology, Pingtung 91201, Taiwan, R.O.C.
Yi-Chun HsiehRegenerative Medicine and Cell Therapy Research Center, Kaohsiung Medical University, Kaohsiung 80708, Taiwan, R.O.C.
Huei-Syuan LiuRegenerative Medicine and Cell Therapy Research Center, Kaohsiung Medical University, Kaohsiung 80708, Taiwan, R.O.C.
Shao-Wei ChenDepartment of Clinical Education and Training, Chung-Ho Memorial Hospital, Kaohsiung Medical University, Kaohsiung 80708, Taiwan, R.O.C.
Yung-Yun HuangDepartment of Anesthesiology, Kaohsiung Veterans General Hospital, Kaohsiung 813414, Taiwan, R.O.C.
Li-Ching LinDivision of General Surgery, Chang Gung Memorial Hospital, New Taipei 33303, Taiwan, R.O.C.
Tsung-Fu TsaiDepartment of Dermatology, Chang Gung Memorial Hospital, New Taipei 33303, Taiwan, R.O.C.
Yun-Fang LiangSchool of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan, R.O.C.
Wen-Li HsuRegenerative Medicine and Cell Therapy Research Center, Kaohsiung Medical University, Kaohsiung 80708, Taiwan, R.O.C.
Kaohsiung Medical University · TWChang Gung Memorial Hospital · TWKaohsiung Medical University Chung-Ho Memorial Hospital · TWKaohsiung Veterans General Hospital · TWNational Cheng Kung University · TWNational Pingtung University of Science and Technology · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transient receptor potential canonical 7 (TRPC7) has been reported to mediate aging-associated tumorigenesis, but the role of TRPC7 in cancer malignancy is still unclear. TRPC7 is associated with tumor size in patients with lung adenocarcinoma and the present study further evaluated the underlying mechanism of TRPC7 in the regulation of cancer progression. The clinicopathological role of TRPC7 was assessed using immunohistochemistry staining and the pathological mechanism of TRPC7 in lung adenocarcinoma cells was determined using cell cycle examination, invasion and calcium response assays, and immunoblot analysis. The results indicated that high TRPC7 expression was associated with a lower 5-year survival rate compared with low TRPC7 expression, which suggested that TRPC7 expression was inversely associated with overall survival in patients with lung adenocarcinoma. TRPC7 serves a pathological role by facilitating the enhancement of cell growth and migration with increased phosphorylation of Ca

Indexed as

Ca2+ signalingcancer cell growthcancer cell migrationlung adenocarcinomatransient receptor potential canonical 7

Identifiers

PMID36817036
PMCPMC9932057
OpenAlexW4317821210

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.