作者
Andrew Storfer, Paul A Hohenlohe, Mark J Margres, Austin Patton, Alexandra K Fraik, Matthew Lawrance, Lauren E Ricci, Amanda R Stahlke, Hamish I McCallum, Menna E Jones
发表日期
2018/8/2
来源
PLoS pathogens
卷号
14
期号
8
页码范围
e1007098
出版商
Public Library of Science
简介
Cancer poses one of the greatest human health threats of our time. Fortunately, aside from a few rare cases of cancer transmission in immune-suppressed organ transplant recipients [1] or a small number of transmission events from mother to fetus [2], cancers are not spread from human to human. However, transmissible cancers have been detected in vertebrate and invertebrate animals, sometimes with devastating effects [3]. Four examples of transmissible cancers are now known: 1) canine transmissible venereal tumor (CTVT) in dogs [4], 2) a tumor in a laboratory population of Syrian hamsters that is no longer cultured [3], 3) infectious neoplasias in at least four species of bivalve mollusks [5, 6], and 4) two independently derived transmissible cancers (devil facial tumor disease [DFTD]) in Tasmanian devils [7–10](Fig 1A and 1B). The etiologic agents of CTVT [4], the bivalve cancers [5], and DFTD [7] are the transplants (allografts) of the neoplastic cells themselves, but the etiologic agent is unknown for the hamster tumor.
The effects of these transmissible cancers on their respective host populations vary. CTVT is spread in dogs through sexual contact and is at least 11,000 years old, placing the timing of its origin close to that of the domestication of dogs [11]. Although genomic analyses of the tumor suggest evasion of multiple components of the dog immune system, dogs most commonly survive and often show evidence of spontaneous tumor regression within a year of initial diagnosis [11, 12]. For the infectious bivalve neoplasias, which have existed for at least 40 years, population effects vary from enzootic infections with no noticeable effects …
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