期刊
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
卷 24, 期 13, 页码 -出版社
MDPI
DOI: 10.3390/ijms241311094
关键词
carbonic anhydrase IX; propranolol; hypoxia; tumor microenvironment; hypoxia inducible factor 1; chemoresistance
Resistance to chemotherapy is a major obstacle in cancer treatment. The non-selective beta-blocker propranolol has the potential to overcome drug resistance by disrupting tumor adaptation and activating apoptosis. It can serve as a chemosensitizer in combined therapy to disrupt tumor microenvironment homeostasis.
Resistance to chemotherapy represents a persisting medical problem, ranking among main causes of chemotherapy failure and cancer mortality. There is a possibility to utilize and repurpose already existing therapeutics which were not primarily intended for oncological treatment. Overactivation of adrenergic receptors and signaling dysregulation promotes tumor progression, metastatic potential, immune system evasion, tumor angiogenesis and drug resistance. The non-selective beta-blocker propranolol, approved in infantile haemangioma treatment, has a high potential for use in cancer therapy. We analyzed the effects of propranolol and 5-fluorouracil combination on sensitive and resistant cells derived from colorectal carcinoma in monolayers, single-component and co-culture spheroids and in vivo mouse models. Our results revealed that propranolol is able to exert its effect not only in chemosensitive colorectal cells, but also in 5-fluorouracil resistant cells. Propranolol disrupts the hypoxic adaptation machinery by inhibiting HIF1 & alpha;, carbonic anhydrase IX, and activates apoptosis, which may be important in the management of chemo-resistant patients. We showed that propranolol slows down the growth of xenografts formed from colorectal cancer cells, even from cells already adapted to the & beta;-blocker. We provide clear evidence that blockade of & beta;-adrenergic receptors affects essential signaling pathways modulating tumor microenvironment and thus the response to anticancer therapy. Our findings indicate that propranolol could be repurposed to serve as chemosensitizer in combined therapy aimed at disrupting homeostasis of tumor microenvironment.
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