Thursday, November 24, 2016

Study shows low-dose chemotherapy regimens could prevent tumor recurrence in some cancers

https://www.eurekalert.org/pub_releases/2016-11/rup-ssl111616.php

Public Release: 23-Nov-2016
Study shows low-dose chemotherapy regimens could prevent tumor recurrence in some cancers
Rockefeller University Press

Conventional, high-dose chemotherapy treatments can cause the fibroblast cells surrounding tumors to secrete proteins that promote the tumors' recurrence in more aggressive forms, researchers at Taipei Medical University and the National Institute of Cancer Research in Taiwan and University of California, San Francisco, have discovered. Frequent, low-dose chemotherapy regimens avoid this effect and may therefore be more effective at treating certain types of breast and pancreatic cancer, according to the murine study "Metronomic chemotherapy prevents therapy-induced stromal activation and induction of tumor-initiating cells," which will be published online November 23 in The Journal of Experimental Medicine.

Chemotherapy drugs are usually administered to cancer patients every few weeks at a high "maximum tolerated" dose. Though this approach kills the majority of tumor cells, it often spares a small number of tumor-initiating cells (TICs) that subsequently give rise to new tumors. Moreover, these recurring tumors are often more aggressive and able to metastasize to other tissues, in part because high doses of chemotherapy drugs also affect cells in the stromal tissue that surrounds tumors, including immune cells and blood vessel endothelial cells.

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Recent studies have suggested that treating patients with low doses of chemotherapy drugs at more frequent, even daily, intervals may be more effective than traditional chemotherapeutic approaches. Tsai and colleagues found that such "low-dose metronomic" regimens did not induce the production of ELR+ chemokines by cancer-associated fibroblasts. This, in turn, reduced the fibroblasts' ability to promote TIC formation, blood vessel growth, and macrophage recruitment.

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