Evidence map›Paper›PMID 27203214›Full record

ArticleOncotarget2016

Down-regulation of tensin2 enhances tumorigenicity and is associated with a variety of cancers.

Shiao-Ya Hong, Yi-Ping Shih, Peng Sun, Wang-Ju Hsieh, Wen-Chang Lin, Su Hao Lo

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. From Plastics to Prognosis:Diagnostics (Basel, Switzerland) · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Genes · 2023
    Article
  7. The molecular and clinical role of Tensin 1/2/3 in cancer.Journal of cellular and molecular medicine · 2023
    Review
  8. Tensins in Kidney Function and Diseases.Life (Basel, Switzerland) · 2023
    Review
  9. The role of tensins in malignant neoplasms.Archives of medical science : AMS · 2023
    Article
  10. Article
  11. The Roles of Pseudophosphatases in Disease.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

6 authors at 2 institutions in 2 countries.

Shiao-Ya HongDepartment of Biochemistry and Molecular Medicine, University of California-Davis, Sacramento, CA 95817, USA.
Yi-Ping ShihDepartment of Biochemistry and Molecular Medicine, University of California-Davis, Sacramento, CA 95817, USA.
Peng SunDepartment of Biochemistry and Molecular Medicine, University of California-Davis, Sacramento, CA 95817, USA.
Wang-Ju HsiehDepartment of Biochemistry and Molecular Medicine, University of California-Davis, Sacramento, CA 95817, USA.
Wen-Chang LinInstitute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Su Hao LoDepartment of Biochemistry and Molecular Medicine, University of California-Davis, Sacramento, CA 95817, USA.
University of California, Davis · USInstitute of Biomedical Sciences, Academia Sinica · TW

Funding

Role of Cten in Prostate CancerR01CA102537 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI LO, SU HAO · 2004 to 2016
$2.4M
Deleted in liver cancer 1 (DLC1) in liver development and diseaseK01DK097291 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SHIH, YI-PING · 2013 to 2016
$471k
Role of Cten in Prostate CancerR56CA102537 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LO, SU HAO · 2009 to 2009
$240k
NCI NIH HHS R01 CA102537NCI NIH HHS R56 CA102537NIDDK NIH HHS K01 DK097291
6 · The paper itself

Abstract

Tensin family members, including tensin2 (TNS2), are present as major components of the focal adhesions. The N-terminal end of TNS2 contains a C1 region (protein kinase C conserved region 1) that is not found in other tensin members. Three isoforms of TNS2 have been identified with previous reports describing the shortest V3 isoform as lacking the C1 region. Although TNS2 is known to regulate cell proliferation and migration, its role in tumorigenicity is controversial. By gain-of-function overexpression approaches, results supporting either promotion or reduction of cancer cell tumorigenicity were reported. Here we report that the complete V3 isoform also contains the C1 region and describe the expression patterns of the three human TNS2 isoforms. By loss-of-function approaches, we show that silencing of TNS2 up-regulates the activities of Akt, Mek, and IRS1, and increases tumorigenicities in A549 and Hela cells. Using public database analyses we found that TNS2 is down-regulated in head and neck, esophageal, breast, lung, liver, and colon cancer. In addition, patients with low TNS2 expression showed poor relapse-free survival rates for breast and lung cancers. These results strongly suggest a role of tensin2 in suppressing cell transformation and reduction of tumorigenicity.

Indexed as

A549 CellsAnimalsCarcinogenesisCell Line, TumorCell ProliferationDown-RegulationFocal AdhesionsHeLa CellsHeterograftsHumansMiceNeoplasmsTensinsTransfectionTensinsTNS2 protein, humanfocal adhesionIRS1Mektensintumorigenesis

Identifiers

PMID27203214
PMCPMC5122378
OpenAlexW2405732702

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.