Evidence map›Paper›PMID 30678233›Full record

ArticleCancers2019

Tribbles Homolog 3 Involved in Radiation Response of Triple Negative Breast Cancer Cells by Regulating Notch1 Activation.

Yueh-Chun Lee, Wen-Ling Wang, Wei-Chao Chang, Yu-Hao Huang, Guan-Ci Hong, Hui-Lin Wang, Ying-Hsiang Chou, Hsien-Chun Tseng, Hsueh-Te Lee, Shao-Ti Li and 5 more

Abstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

24 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Notch Signalling in Breast Development and Cancer.Frontiers in cell and developmental biology · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. TRIB3 promotes hepatocellular carcinoma growth and predicts poor prognosis.Cancer biomarkers : section A of Disease markers · 2020
    Observational
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

15 authors.

Yueh-Chun LeeDepartment of Radiation Oncology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan. lee.yuehchun@gmail.com.
Wen-Ling WangSchool of Biomedical Sciences, Chung Shan Medical University, Taichung 40201, Taiwan. u8966003.lin@gmail.com.
Wei-Chao ChangGraduate Institute of Biomedical Sciences and Center for Molecular Medicine, China Medical University, Taichung 40402, Taiwan. proma@mail.cmu.edu.tw.
Yu-Hao HuangSchool of Biomedical Sciences, Chung Shan Medical University, Taichung 40201, Taiwan. bms0217062@gmail.com.
Guan-Ci HongSchool of Biomedical Sciences, Chung Shan Medical University, Taichung 40201, Taiwan. cream8515@gmail.com.
Hui-Lin WangSchool of Biomedical Sciences, Chung Shan Medical University, Taichung 40201, Taiwan. huilin117@gmail.com.
Ying-Hsiang ChouDepartment of Radiation Oncology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan. hideka.chou@gmail.com.ORCID 0000-0001-5888-4302
Hsien-Chun TsengDepartment of Radiation Oncology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan. rad.tseng@msa.hinet.net.
Hsueh-Te LeeInstitute of Anatomy and Cell Biology, School of Medicine, National Yang Ming University, Taipei 11221, Taiwan. incubator.lee@ym.edu.tw.ORCID 0000-0002-9152-2618
Shao-Ti LiDepartment of Radiation Oncology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan. showtear@gmail.com.
Hsin-Lin ChenDepartment of Radiation Oncology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan. cznpzz@gmail.com.
Chun-Chieh WuDepartment of Radiation Oncology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan. kubernet332@gmail.com.
Huei-Fan YangDepartment of Radiation Oncology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan. benlinda.tw@yahoo.com.tw.
Bing-Yen WangDivision of Thoracic Surgery, Department of Surgery, Changhua Christian Hospital, Changhua City 50006, Taiwan. 156283@cch.org.tw.
Wen-Wei ChangSchool of Biomedical Sciences, Chung Shan Medical University, Taichung 40201, Taiwan. changww@csmu.edu.tw.ORCID 0000-0003-2283-1377

Funding

Chung Shan Medical University Hospital CSH-2017-C-035Ministry of Science and Technology, R.O.C MOST 106-2314-B-040-024-MY3 and MOST 107-2310-B-040-009-MY3
6 · The paper itself

Abstract

Breast cancer is the most common cancer for women in Taiwan and post-lumpectomy radiotherapy is one of the therapeutic strategies for this malignancy. Although the 10-year overall survival of breast cancer patients is greatly improved by radiotherapy, the locoregional recurrence is around 10% and triple negative breast cancers (TNBCs) are at a high risk for relapse. The aim of this paper is to understand the mechanisms of radioresistance in breast cancers which may facilitate the development of new treatments in sensitizing breast cancer toward radiation therapy. Tribbles homolog 3 (TRIB3) is a pseudokinase protein and known to function as a protein scaffold within cells. It has been reported that higher TRIB3 expression is a poor prognostic factor in breast cancer patients with radiotherapy. In this study, we investigate the involvement of TRIB3 in the radiation response of TNBC cells. We first found that the expression of TRIB3 and the activation of Notch1, as well as Notch1 target genes, increased in two radioresistant TNBC cells. Knockdown of TRIB3 in radioresistant MDA-MB-231 TNBC cells decreased Notch1 activation, as well as the CD24-CD44⁺ cancer stem cell population, and sensitized cells toward radiation treatment. The inhibitory effects of TRIB3 knockdown in self-renewal or radioresistance could be reversed by forced expression of the Notch intracellular domain. We also observed an inhibition in cell growth and accumulated cells in the G₀/G¹ phase in radioresistant MDA-MB-231 cells after knockdown of TRIB3. With immunoprecipitation and mass spectrometry analysis, we found that, BCL2-associated transcription factor 1 (BCLAF1), BCL2 interacting protein 1 (BNIP1), or DEAD-box helicase 5 (DDX5) were the possible TRIB3 interacting proteins and immunoprecipitation data also confirmed that these proteins interacted with TRIB3 in radioresistant MDA-MB-231 cells. In conclusion, the expression of TRIB3 in radioresistant TNBC cells participated in Notch1 activation and targeted TRIB3 expression may be a strategy to sensitize TNBC cells toward radiation therapy.

Indexed as

Notch1radioresistanceTRIB3triple negative breast cancer

Identifiers

PMID30678233
PMCPMC6406679

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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.