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Open AccessEditorial

Targeting STAT3 and STAT5 in Cancer

1
Centre for Medicinal Chemistry, University of Toronto at Mississauga, Mississauga, ON L5L 1C6, Canada
2
Department of Chemical and Physical Sciences, University of Toronto at Mississauga, Mississauga, ON L5L 1C6, Canada
3
Medicinal Chemistry, Research Center for Natural Sciences, 1117 Budapest, Hungary
4
Institute of Animal Breeding and Genetics, University of Veterinary Medicine, A-1210 Vienna, Austria
*
Author to whom correspondence should be addressed.
Cancers 2020, 12(8), 2002; https://doi.org/10.3390/cancers12082002
Received: 15 July 2020 / Accepted: 16 July 2020 / Published: 22 July 2020
(This article belongs to the Special Issue Targeting STAT3 and STAT5 in Cancer)
Note: In lieu of an abstract, this is an excerpt from the first page.

Insights into the mutational landscape of the human cancer genome coding regions defined about 140 distinct cancer driver genes in 2013, which approximately doubled to 300 in 2018 following advances in systems cancer biology studies [...] View Full-Text
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MDPI and ACS Style

de Araujo, E.D.; Keserű, G.M.; Gunning, P.T.; Moriggl, R. Targeting STAT3 and STAT5 in Cancer. Cancers 2020, 12, 2002. https://doi.org/10.3390/cancers12082002

AMA Style

de Araujo ED, Keserű GM, Gunning PT, Moriggl R. Targeting STAT3 and STAT5 in Cancer. Cancers. 2020; 12(8):2002. https://doi.org/10.3390/cancers12082002

Chicago/Turabian Style

de Araujo, Elvin D.; Keserű, György M.; Gunning, Patrick T.; Moriggl, Richard. 2020. "Targeting STAT3 and STAT5 in Cancer" Cancers 12, no. 8: 2002. https://doi.org/10.3390/cancers12082002

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