Senescent cells promote breast cancer cells motility by secreting GM-CSF and bFGF that activate the JNK signaling pathway

Bibliographic Details
Title: Senescent cells promote breast cancer cells motility by secreting GM-CSF and bFGF that activate the JNK signaling pathway
Authors: Nan Wang, Yan Fang, Yigong Hou, Dongmei Cheng, Emily V. Dressler, Hao Wang, Juan Wang, Guanwen Wang, Yilei Li, Hong Liu, Rong Xiang, Shuang Yang, Peiqing Sun
Source: Cell Communication and Signaling, Vol 22, Iss 1, Pp 1-13 (2024)
Publisher Information: BMC, 2024.
Publication Year: 2024
Collection: LCC:Medicine
LCC:Cytology
Subject Terms: Breast cancer, Metastasis, Senescence, Migration, GM-CSF, bFGF, Medicine, Cytology, QH573-671
More Details: Abstract Background Cellular senescence can be induced in mammalian tissues by multiple stimuli, including aging, oncogene activation and loss of tumor suppressor genes, and various types of stresses. While senescence is a tumor suppressing mechanism when induced within premalignant or malignant tumor cells, senescent cells can promote cancer development through increased secretion of growth factors, cytokines, chemokines, extracellular matrix, and degradative enzymes, collectively known as senescence-associated secretory phenotype (SASP). Previous studies indicated that senescent cells, through SASP factors, stimulate tumor cell invasion that is a critical step in cancer cell metastasis. Methods In the current study, we investigated the effect of senescent cells on the motility of breast cancer cells, which is another key step in cancer cell metastasis. We analyzed the motility of breast cancer cells co-cultured with senescent cells in vitro and metastasis of the breast cancer cells co-injected with senescent cells in orthotopic xenograft models. We also delineated the signaling pathway mediating the effect of senescent cells on cancer cell motility. Results Our results indicate that senescent cells stimulated the migration of breast cancer cells through secretion of GM-CSF and bFGF, which in turn induced activation of the JNK pathway in cancer cells. More importantly, senescent cells promoted breast cancer metastasis, with a minimum effect on the primary tumor growth, in orthotopic xenograft mouse models. Conclusions These results have revealed an additional mechanism by which senescent cells promote tumor cell metastasis and tumor progression, and will potentially lead to identification of novel targets for cancer therapies that suppress metastasis, the major cause of cancer mortality.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1478-811X
Relation: https://doaj.org/toc/1478-811X
DOI: 10.1186/s12964-024-01861-x
Access URL: https://doaj.org/article/0e0435df319e490f94c929e8a4085c83
Accession Number: edsdoj.0e0435df319e490f94c929e8a4085c83
Database: Directory of Open Access Journals
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More Details
ISSN:1478811X
DOI:10.1186/s12964-024-01861-x
Published in:Cell Communication and Signaling
Language:English