| Literature DB >> 33669052 |
Beate Heissig1, Yousef Salama2, Taro Osada3, Ko Okumura1, Koichi Hattori4.
Abstract
Fibrinolytic factors like plasminogen, tissue-type plasminogen activator (tPA), and urokinase plasminogen activator (uPA) dissolve clots. Though mere extracellular-matrix-degrading enzymes, fibrinolytic factors interfere with many processes during primary cancer growth and metastasis. Their many receptors give them access to cellular functions that tumor cells have widely exploited to promote tumor cell survival, growth, and metastatic abilities. They give cancer cells tools to ensure their own survival by interfering with the signaling pathways involved in senescence, anoikis, and autophagy. They can also directly promote primary tumor growth and metastasis, and endow tumor cells with mechanisms to evade myelosuppression, thus acquiring drug resistance. In this review, recent studies on the role fibrinolytic factors play in metastasis and controlling cell-death-associated processes are presented, along with studies that describe how cancer cells have exploited plasminogen receptors to escape myelosuppression.Entities:
Keywords: LRP1; anoikis; cancer; drug resistance; exosomes; metastasis; plasminogen; premetastatic niche; senescence; uPAR
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Year: 2021 PMID: 33669052 PMCID: PMC7956603 DOI: 10.3390/ijms22052304
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923