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pmid:33298901

BMP signaling is a therapeutic target in ovarian cancer.

Tomohiko Fukuda · Risa Fukuda · Ryo Tanabe · Daizo Koinuma · Hiroo Koyama · Yoshinobu Hashizume · Aristidis Moustakas · Kohei Miyazono · Carl-Henrik Heldin

Cell death discovery · 2020 doi:10.1038/s41420-020-00377-w

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:33298901
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title
BMP signaling is a therapeutic target in ovarian cancer.
doi
10.1038/s41420-020-00377-w
pmid
33298901
authors array · 9 items
[0]
Tomohiko Fukuda
[1]
Risa Fukuda
[2]
Ryo Tanabe
[3]
Daizo Koinuma
[4]
Hiroo Koyama
[5]
Yoshinobu Hashizume
[6]
Aristidis Moustakas
[7]
Kohei Miyazono
[8]
Carl-Henrik Heldin
journal
Cell death discovery
year
2020
abstract
BMP signaling has been found to have tumor-promoting as well as tumor-suppressing effects in different types of tumors. In this study, we investigated the effects of BMP signaling and of BMP inhibitors on ovarian cancer (OC) cells in vitro and in vivo. High expression of BMP receptor 2 (BMPR2) correlated with poor overall survival of OC patients in the TCGA dataset. Both BMP2 and BMPR2 enhanced OC cell proliferation, whereas BMP receptor kinase inhibitors inhibited OC cell growth in cell culture as well as in a mouse model. BMP2 also augmented sphere formation, migration, and invasion of OC cells, and induced EMT. High BMP2 expression was observed after chemotherapy of OC patients in the GSE109934 dataset. In accordance, carboplatin, used for the treatment of OC patients, increased BMP2 secretion from OC cells, and induced EMT partially via activation of BMP signaling. Our data suggest that BMP signaling has tumor-promoting effects in OC, and that BMP inhibitors might be useful therapeutic agents for OC patients. Considering that carboplatin treatment augmented BMP2 secretion, the possibility to use a combination of BMP inhibitors and carboplatin in the treatment of OC patients, would be worth exploring.
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The significance of differences between more than three samples was analyzed by one-way ANOVA with Tukey test, whereas the significance between two samples was analyzed by two-tailed Student’s t-test.
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Gene expression profiles of OC samples were obtained from cBioPortal (TCGA serous ovarian cancer) and GEO database (GSE109934)23,42. We analyzed the TCGA serous ovarian cancer dataset, which contained RNA-Seq data of 306 patients via submitting a query to cBioPortal23,43,44.
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Gene expression profiles of OC samples were obtained from cBioPortal (TCGA serous ovarian cancer) and GEO database (GSE109934)23,42. We analyzed the TCGA serous ovarian cancer dataset, which contained RNA-Seq data of 306 patients via submitting a query to cBioPortal23,43,44.
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Gene expression profiles of OC samples were obtained from cBioPortal (TCGA serous ovarian cancer) and GEO database (GSE109934)23,42. We analyzed the TCGA serous ovarian cancer dataset, which contained RNA-Seq data of 306 patients via submitting a query to cBioPortal23,43,44.
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Molecular Response to Neoadjuvant Chemotherapy in High-Grade Serous Ovarian Carcinoma
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Gene expression profiles of OC samples were obtained from cBioPortal (TCGA serous ovarian cancer) and GEO database (GSE109934)23,42. We analyzed the TCGA serous ovarian cancer dataset, which contained RNA-Seq data of 306 patients via submitting a query to cBioPortal23,43,44.
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Gene expression profiles of OC samples were obtained from cBioPortal (TCGA serous ovarian cancer) and GEO database (GSE109934)23,42. We analyzed the TCGA serous ovarian cancer dataset, which contained RNA-Seq data of 306 patients via submitting a query to cBioPortal23,43,44.
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Gene expression profiles of OC samples were obtained from cBioPortal (TCGA serous ovarian cancer) and GEO database (GSE109934)23,42. We analyzed the TCGA serous ovarian cancer dataset, which contained RNA-Seq data of 306 patients via submitting a query to cBioPortal23,43,44.
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cell growth in cell culture as well as in a mouse model. BMP2 also augmented sphere formation, migra
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cell growth in cell culture as well as in a mouse model. BMP2 also augmented sphere formation,
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33298901", "kind": "science-record", "revision": 9, "content_hash": "sha256:6031d4e9da6a93b69d05a771e8489390b492e62d2433a8fdf4039e593dc31d5a", "created_at": "2026-11-01T15:41:18Z", "updated_at": "2026-11-01T22:45:46Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "BMP signaling is a therapeutic target in ovarian cancer.", "doi": "10.1038/s41420-020-00377-w", "pmid": "33298901", "authors": ["Tomohiko Fukuda", "Risa Fukuda", "Ryo Tanabe", "Daizo Koinuma", "Hiroo Koyama", "Yoshinobu Hashizume", "Aristidis Moustakas", "Kohei Miyazono", "Carl-Henrik Heldin"], "journal": "Cell death discovery", "year": 2020, "abstract": "BMP signaling has been found to have tumor-promoting as well as tumor-suppressing effects in different types of tumors. In this study, we investigated the effects of BMP signaling and of BMP inhibitors on ovarian cancer (OC) cells in vitro and in vivo. High expression of BMP receptor 2 (BMPR2) correlated with poor overall survival of OC patients in the TCGA dataset. Both BMP2 and BMPR2 enhanced OC cell proliferation, whereas BMP receptor kinase inhibitors inhibited OC cell growth in cell culture as well as in a mouse model. BMP2 also augmented sphere formation, migration, and invasion of OC cells, and induced EMT. High BMP2 expression was observed after chemotherapy of OC patients in the GSE109934 dataset. In accordance, carboplatin, used for the treatment of OC patients, increased BMP2 secretion from OC cells, and induced EMT partially via activation of BMP signaling. Our data suggest that BMP signaling has tumor-promoting effects in OC, and that BMP inhibitors might be useful therapeutic agents for OC patients. Considering that carboplatin treatment augmented BMP2 secretion, the possibility to use a combination of BMP inhibitors and carboplatin in the treatment of OC patients, would be worth exploring.", "claims": [{"id": "claim-method", "statement": "The significance of differences between more than three samples was analyzed by one-way ANOVA with Tukey test, whereas the significance between two samples was analyzed by two-tailed Student’s t-test.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33298901", "locator": "sections[27] \"Statistical analysis\" paragraph 2", "quote": "The significance of differences between more than three samples was analyzed by one-way ANOVA with Tukey test, whereas the significance between two samples was analyzed by two-tailed Student’s t-test."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Gene expression profiles of OC samples were obtained from cBioPortal (TCGA serous ovarian cancer) and GEO database (GSE109934)23,42. 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