Evidence map›Paper›PMID 36651490›Full record

ArticleJournal of cellular and molecular medicine2023

Pirfenidone suppressed triple-negative breast cancer metastasis by inhibiting the activity of the TGF-β/SMAD pathway.

Daiqin Luo, Xianlin Zeng, Shuling Zhang, Daohong Li, Zhimei Cheng, Yun Wang, Jinhua Long, Zuquan Hu, Shiqi Long, Jing Zhou and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 25 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Daiqin LuoSchool of Basic Medical Sciences/School of Biology & Engineering, Guizhou Medical University, Guiyang, China.ORCID 0000-0002-6045-3971
Xianlin ZengSchool of Basic Medical Sciences/School of Biology & Engineering, Guizhou Medical University, Guiyang, China.
Shuling ZhangSchool of Public Health, Guizhou Medical University, Guiyang, China.
Daohong LiSchool of Basic Medical Sciences/School of Biology & Engineering, Guizhou Medical University, Guiyang, China.
Zhimei ChengDepartment of Interventional Radiology, Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Yun WangSchool of Basic Medical Sciences/School of Biology & Engineering, Guizhou Medical University, Guiyang, China.
Jinhua LongSchool of Basic Medical Sciences/School of Biology & Engineering, Guizhou Medical University, Guiyang, China.
Zuquan HuSchool of Basic Medical Sciences/School of Biology & Engineering, Guizhou Medical University, Guiyang, China.
Shiqi LongSchool of Basic Medical Sciences/School of Biology & Engineering, Guizhou Medical University, Guiyang, China.
Jing ZhouSchool of Basic Medical Sciences/School of Biology & Engineering, Guizhou Medical University, Guiyang, China.
Shuai ZhangDepartment of Interventional Radiology, Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Zhu ZengSchool of Basic Medical Sciences/School of Biology & Engineering, Guizhou Medical University, Guiyang, China.
Guiyang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among breast cancer patients, metastases are the leading cause of death. Despite decades of effort, little progress has been made to improve the treatment of breast cancer metastases, especially triple-negative breast cancer (TNBC). The extracellular matrix plays an important role in tumour growth and metastasis by causing its deposition, remodelling, and signalling. As we know, the process of fibrosis results in excessive amounts of extracellular matrix being deposited within the cells. So, it will be interesting to study if the use of anti-fibrotic drugs in combination with conventional chemotherapy drugs can produce synergistic antitumor effects. In this study, we assessed the efficacy of Pirfenidone (PFD), an FDA-approved medication for the treatment of idiopathic pulmonary fibrosis, on TNBC cells as well as its anti-tumour effects in xenograft tumour model. PFD inhibited in a dose-dependent manner breast cancer cell proliferation, migration, and invasion, while promoted their apoptosis in vitro. PFD also suppressed TGF-β-induced activation of Smad signalling pathway and expression level of EMT-inducing transcription factors (e.g. SNAI2, TWIST1, ZEB1) as well as the mesenchymal genes such as VIMENTIN and N-Cadherin. On the contrary, the expression level of epithelial marker gene E-Cadherin was up-regulated in the presence of PFD. In vivo, PFD alone exerted a milder but significant anti-tumour effect than the chemotherapy drug nanoparticle albumin-bound paclitaxel (nab-PTX) did in the breast cancer xenograft mouse model. Interestingly, PFD synergistically boosted the cancer-killing effect of nab-PTX. Furthermore, Our data suggest that PFD suppressed breast cancer metastasis by inhibiting the activity of the TGFβ/SMAD pathway.

Indexed as

Transforming Growth Factor betaTriple Negative Breast NeoplasmsAnimalsCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionHumansMicePyridonesSignal TransductionSmad ProteinspirfenidonePyridonesSmad ProteinsTransforming Growth Factor betabreast cancerEMTmetastasisPirfenidoneTGF-β

Identifiers

PMID36651490
PMCPMC9889661
OpenAlexW4317360496

What OpenQuestion holds

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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.