Evidence map›Paper›PMID 34608584›Full record

ArticleJournal of cell communication and signaling2022

BMP4 enhances anoikis resistance and chemoresistance of breast cancer cells through canonical BMP signaling.

Renu Sharma, Gayatri Gogoi, Snigdha Saikia, Amit Sharma, Deep Jyoti Kalita, Anupam Sarma, Anil Mukund Limaye, Manish Kumar Gaur, Jina Bhattacharyya, Bithiah Grace Jaganathan

Open access · greenAbstract read
In one paragraph

Article in Journal of cell communication and signaling, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

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  16. Anoikis patterns via machine learning strategy and experimental verification exhibit distinct prognostic and immune landscapes in melanoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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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

10 authors at 5 institutions in 1 country.

Renu SharmaStem Cells and Cancer Biology Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, India.
Gayatri GogoiDepartment of Pathology, Assam Medical College, Dibrugarh, Assam, India.
Snigdha SaikiaDepartment of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India.
Amit SharmaStem Cells and Cancer Biology Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, India.
Deep Jyoti KalitaDepartment of Surgical Oncology, Dr B. Borooah Cancer Institute, Guwahati, Assam, India.
Anupam SarmaDepartment of Oncopathology, Dr B. Borooah Cancer Institute, Guwahati, Assam, India.
Anil Mukund LimayeDepartment of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India.
Manish Kumar GaurDepartment of Surgical Oncology, All India Institute of Medical Sciences, New Delhi, India.
Jina BhattacharyyaDepartment of Hematology, Gauhati Medical College, Guwahati, Assam, India.
Bithiah Grace JaganathanStem Cells and Cancer Biology Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, India. bithiahgj@iitg.ac.in.ORCID http://orcid.org/0000-0002-5955-1371
Indian Institute of Technology Guwahati · INBhubaneswar Borooah Cancer Institute · INAll India Institute of Medical Sciences · INAssam Medical College · INGauhati Medical College and Hospital · IN

Funding

indian council of medical research 05/07/1502/2016-CHscience and engineering research board EMR/2015/002096
6 · The paper itself

Abstract

Bone morphogenetic proteins (BMPs) regulate cell fate during development and mediate cancer progression. In this study, we investigated the role of BMP4 in proliferation, anoikis resistance, metastatic migration, and drug resistance of breast cancer cells. We utilized breast cancer cell lines and clinical samples representing different subtypes to understand the functional effect of BMP4 on breast cancer. The BMP pathway was inhibited with the small molecule inhibitor LDN193189 hydrochloride (LDN). BMP4 signaling enhanced the expression of stem cell genes CD44, ALDH1A3, anti-apoptotic gene BCL2 and promoted anoikis resistance in MDA-MB-231 breast cancer cells. BMP4 enhanced self-renewal and chemoresistance in MDA-MB-231 by upregulating Notch signaling while LDN treatment abrogated anoikis resistance and proliferation of anoikis resistant breast cancer cells in the osteogenic microenvironment. Conversely, BMP4 downregulated proliferation, colony-forming ability, and suppressed anoikis resistance in MCF7 and SkBR3 cells, while LDN treatment promoted tumor spheroid formation and growth. These findings indicate that BMP4 has a context-dependent role in breast cancer. Further, our data with MDA-MB-231 cells representing triple-negative breast cancer suggest that BMP inhibition might impair its metastatic spread and colonization.

Indexed as

anoikis resistancecancer stem cellschemoresistanceMetastatic migrationTNBC

Identifiers

PMID34608584
PMCPMC8891411
OpenAlexW3203165279

What OpenQuestion 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 OpenQuestion graph.