4.7 Article

Molecular characterization of a marine turtle tumor epizootic, profiling external, internal and postsurgical regrowth tumors

Journal

COMMUNICATIONS BIOLOGY
Volume 4, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s42003-021-01656-7

Keywords

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Funding

  1. Sea Turtle Conservancy, Florida Sea Turtle Grants Program [17-033R]
  2. Save Our Seas Foundation [SOSF 356]
  3. National Save The Sea Turtle Foundation, Inc.
  4. Welsh Government Ser Cymru II
  5. European Union [663830-BU115]
  6. Gumbo Limbo Nature Center, Inc d/b/a Friends of Gumbo Limbo (a 501c3 non-profit organization)
  7. Irish Research Council Government of Ireland Postgraduate Scholarship [GOIPG/2020/1056]
  8. Gates Cambridge PhD scholarship
  9. University of Texas Rio Grande Valley Transforming Our World Strategic Plan

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Sea turtle populations are threatened by fibropapillomatosis, an animal epidemic. Researchers have found that internal tumors in turtles with this disease are molecularly distinct from external tumors, though they share common oncogenic signaling pathways that could be targeted for treatment.
Sea turtle populations are under threat from an epizootic tumor disease (animal epidemic) known as fibropapillomatosis. Fibropapillomatosis continues to spread geographically, with prevalence of the disease also growing at many longer-affected sites globally. However, we do not yet understand the precise environmental, mutational and viral events driving fibropapillomatosis tumor formation and progression.Here we perform transcriptomic and immunohistochemical profiling of five fibropapillomatosis tumor types: external new, established and postsurgical regrowth tumors, and internal lung and kidney tumors. We reveal that internal tumors are molecularly distinct from the more common external tumors. However, they have a small number of conserved potentially therapeutically targetable molecular vulnerabilities in common, such as the MAPK, Wnt, TGF beta and TNF oncogenic signaling pathways. These conserved oncogenic drivers recapitulate remarkably well the core pan-cancer drivers responsible for human cancers. Fibropapillomatosis has been considered benign, but metastatic-related transcriptional signatures are strongly activated in kidney and established external tumors. Tumors in turtles with poor outcomes (died/euthanized) have genes associated with apoptosis and immune function suppressed, with these genes providing putative predictive biomarkers.Together, these results offer an improved understanding of fibropapillomatosis tumorigenesis and provide insights into the origins, inter-tumor relationships, and therapeutic treatment for this wildlife epizootic. Yetsko, Farrell, Duffy, and colleagues conduct transcriptomic and immunohistological profiling of tumors from sea turtles with fibropapillomatosis. Internal tumors are distinct from more common external tumors, but share some oncogenic signaling pathways that may serve as treatment targets in future.

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