Evidence map›Paper›PMID 32650570›Full record

ArticleCancers2020

TIAM2S Mediates Serotonin Homeostasis and Provokes a Pro-Inflammatory Immune Microenvironment Permissive for Colorectal Tumorigenesis.

Ya-Ling Chan, Wei-Chung Lai, Jia-Shing Chen, Joseph Ta-Chien Tseng, Pei-Chin Chuang, Jonathan Jou, Chung-Ta Lee, H Sunny Sun

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Cancer and neurotransmitter receptors.Chinese medical journal · 2025
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Serotonin Pathway in Cancer.International journal of molecular sciences · 2021
    Review
  17. 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

8 authors at 4 institutions in 2 countries.

Ya-Ling ChanDepartment of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan 701, Taiwan.
Wei-Chung LaiInstitute of Molecular Medicine, College of Medicine, National Cheng Kung University, Tainan 701, Taiwan.
Jia-Shing ChenSchool of Medicine for International Students, I-Shou University, Kaohsiung 840, Taiwan.
Joseph Ta-Chien TsengDepartment of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan 701, Taiwan.
Pei-Chin ChuangDepartment of Medical Research, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Jonathan JouDepartment of Surgery, University of Illinois, College of Medicine at Peoria, Peoria, IL 61605, USA.
Chung-Ta LeeDepartment of Pathology, College of Medicine, National Cheng Kung University, Tainan 701, Taiwan.
H Sunny SunInstitute of Molecular Medicine, College of Medicine, National Cheng Kung University, Tainan 701, Taiwan.ORCID 0000-0002-3661-4448
National Cheng Kung University · TWIllinois College · USI-Shou University · TWKaohsiung Chang Gung Memorial Hospital · TW

Funding

Ministry of Science and Technology, Taiwan MOST 103-2321-B-006 -021 -
6 · The paper itself

Abstract

The short isoform of human TIAM2 has been shown to promote proliferation and invasion in various cancer cells. However, the roles of TIAM2S in immune cells in relation to tumor development have not been investigated. To characterize the effects of TIAM2S, we generated TIAM2S-overexpressing mouse lines and found that aged TIAM2S-transgenic (TIAM2S-TG) developed significantly higher occurrence of lymphocytic infiltration and tumorigenesis in various organs, including colon. In addition, TIAM2S-TG is more sensitized to AOM-induced colon tumor development, suggesting a priming effect toward tumorigenesis. In the light of our recent findings that TIAM2S functions as a novel regulator of cellular serotonin level, we found that serotonin, in addition to Cox2, is a unique inflammation marker presented in the colonic lesion sites in the aged TG animals. Furthermore, our results demonstrated that ectopic TIAM2S altered immunity via the expansion of T lymphocytes; this was especially pronounced in CD8

Indexed as

chronic inflammationinflammatory bowel diseaseserotoninT-cell lymphoma invasion and metastasis 2T lymphocyte

Identifiers

PMID32650570
PMCPMC7408714
OpenAlexW3042130451

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.