Evidence map›Paper›PMID 31142739›Full record

ArticleCell death & disease2019

Identification of TC2N as a novel promising suppressor of PI3K-AKT signaling in breast cancer.

Xiang-Lin Hao, Li-Yun Gao, Xiao-Juan Deng, Fei Han, Hong-Qiang Chen, Xiao Jiang, Wen-Bin Liu, Dan-Dan Wang, Jian-Ping Chen, Zhi-Hong Cui and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Novel CandidateCancers · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Xiang-Lin HaoInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.ORCID http://orcid.org/0000-0002-7583-8233
Li-Yun GaoSchool of Public Health, Xinxiang Medical University, Xinxiang, PR China.
Xiao-Juan DengInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.
Fei HanInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.
Hong-Qiang ChenInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.
Xiao JiangInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.
Wen-Bin LiuInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.
Dan-Dan WangInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.
Jian-Ping ChenInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.
Zhi-Hong CuiInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.
Lin AoInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China.
Jia CaoInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China. caojia1962@126.com.
Jin-Yi LiuInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, 400038, PR China. jinyiliutmmu@163.com.ORCID http://orcid.org/0000-0003-1803-7752
Army Medical University · CNXinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although TC2N has proven to be an oncogene in lung cancer, its biological function and molecular mechanisms in other cancer still remains unclear. Here, we investigate in breast cancer that TC2N expression is sharply overexpressed in breast cancer specimens compared with normal breast specimens, and the low TC2N expression was associated with advanced stage, lymphatic metastasis, larger tumors and shorter survival time. Upregulation of TC2N significantly restrains breast cancer cell proliferation in vitro and tumor growth in vivo. Mechanistically, TC2N blocks AKT signaling in a PI3K dependent and independent way through weakening the interaction between ALK and p55γ or inhibiting the binding of EBP1 and AKT. To sum up, these results unmask an ambivalent role of TC2N in cancer, providing a promising inhibitor for PI3K-AKT signaling.

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingAdultAnimalsBreast NeoplasmsCell Line, TumorCell ProliferationFemaleHumansKaplan-Meier EstimateMiceMice, NudeMiddle AgedNuclear ProteinsPhosphatidylinositol 3-KinasesPrognosisAdaptor Proteins, Signal TransducingNuclear ProteinsPA2G4 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA-Binding ProteinsRNA, Small Interfering

Identifiers

PMID31142739
PMCPMC6541591
OpenAlexW2947228598

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.