Evidence map›Paper›PMID 33654196›Full record

ArticleOncogene2021

Tektin4 loss promotes triple-negative breast cancer metastasis through HDAC6-mediated tubulin deacetylation and increases sensitivity to HDAC6 inhibitor.

Li-Ping Ge, Xi Jin, Yun-Song Yang, Xi-Yu Liu, Zhi-Ming Shao, Gen-Hong Di, Yi-Zhou Jiang

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Research progress on lysine acetylation (Review).International journal of molecular medicine · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Role of HDAC6 in carcinomas.Discover oncology · 2026
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Organoids in breast cancer translational research: intersection of technologies.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2025
    Review
  14. Reversible Acetylation of Non-histone Proteins in Human Cancers.Results and problems in cell differentiation · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

7 authors at 3 institutions in 1 country.

Li-Ping Ge *Department of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, PR China.ORCID http://orcid.org/0000-0002-3578-0073
Xi Jin *Department of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, PR China.
Yun-Song YangDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, PR China.
Xi-Yu LiuDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, PR China.
Zhi-Ming ShaoDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, PR China.
Gen-Hong DiDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, PR China. genhongdi@163.com.ORCID http://orcid.org/0000-0003-1482-0643
Yi-Zhou JiangDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, PR China. yizhoujiang@fudan.edu.cn.ORCID http://orcid.org/0000-0003-3699-2630
Fudan University Shanghai Cancer Center · CNShanghai Medical College of Fudan University · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progression of triple-negative breast cancer (TNBC) constitutes a major unresolved clinical challenge, and effective targeted therapies are lacking. Because microtubule dynamics play pivotal roles in breast cancer metastasis, we performed RNA sequencing on 245 samples from TNBC patients to characterize the landscape of microtubule-associated proteins (MAPs). Here, our transcriptome analyses revealed that low expression of one MAP, tektin4, indicated poor patient outcomes. Tektin4 loss led to a marked increase in TNBC migration, invasion, and metastasis and a decrease in microtubule stability. Mechanistically, we identified a novel microtubule-associated complex containing tektin4 and histone deacetylase 6 (HDAC6). Tektin4 loss increased the interaction between HDAC6 and α-tubulin, thus decreasing microtubule stability through HDAC6-mediated tubulin deacetylation. Significantly, we found that tektin4 loss sensitized TNBC cells, xenograft models, and patient-derived organoid models to the HDAC6-selective inhibitor ACY1215. Furthermore, tektin4 expression levels were positively correlated with microtubule stability levels in clinical samples. Together, our findings uncover a metastasis suppressor function of tektin4 and support clinical development of HDAC6 inhibition as a new therapeutic strategy for tektin4-deficient TNBC patients.

Indexed as

AcetylationAnimalsCell MovementCell ProliferationDisease Models, AnimalExome SequencingGene Expression Regulation, NeoplasticHeterograftsHistone Deacetylase 6Histone Deacetylase InhibitorsHumansHydroxamic AcidsMiceMicrotubule ProteinsNeoplasm MetastasisPyrimidinesHDAC6 protein, humanHistone Deacetylase 6Histone Deacetylase InhibitorsHydroxamic AcidsMicrotubule ProteinsPyrimidinesricolinostattektinsTubulin

Identifiers

PMID33654196
OpenAlexW3134690129

What Socratic holds

Textmetadata
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 Socratic graph.