Author
Listed:
- Dane Cheasley
(Peter MacCallum Cancer Centre)
- Matthew J. Wakefield
(Walter and Eliza Hall Institute
The University of Melbourne)
- Georgina L. Ryland
(Peter MacCallum Cancer Centre)
- Prue E. Allan
(Peter MacCallum Cancer Centre)
- Kathryn Alsop
(Peter MacCallum Cancer Centre
The University of Melbourne)
- Kaushalya C. Amarasinghe
(Peter MacCallum Cancer Centre)
- Sumitra Ananda
(Peter MacCallum Cancer Centre
Western Health)
- Michael S. Anglesio
(University of British Columbia)
- George Au-Yeung
(Peter MacCallum Cancer Centre
The University of Melbourne)
- Maret Böhm
(Kinghorn Cancer Centre and Garvan Institute of Medical Research)
- David D. L. Bowtell
(Peter MacCallum Cancer Centre
The University of Melbourne)
- Alison Brand
(University of Sydney)
- Georgia Chenevix-Trench
(Queensland Institute of Medical Research)
- Michael Christie
(The University of Melbourne
Royal Melbourne Hospital)
- Yoke-Eng Chiew
(University of Sydney)
- Michael Churchman
(University of Edinburgh)
- Anna DeFazio
(University of Sydney)
- Renee Demeo
(Peter MacCallum Cancer Centre)
- Rhiannon Dudley
(Hudson Institute of Medical Research)
- Nicole Fairweather
(Hudson Institute of Medical Research)
- Clare G. Fedele
(Peter MacCallum Cancer Centre
The University of Melbourne)
- Sian Fereday
(Peter MacCallum Cancer Centre
The University of Melbourne)
- Stephen B. Fox
(Peter MacCallum Cancer Centre
The University of Melbourne)
- C Blake Gilks
(University of British Columbia)
- Charlie Gourley
(University of Edinburgh)
- Neville F. Hacker
(The University of New South Wales)
- Alison M. Hadley
(Royal Brisbane and Womens Hospital)
- Joy Hendley
(Peter MacCallum Cancer Centre)
- Gwo-Yaw Ho
(Walter and Eliza Hall Institute)
- Siobhan Hughes
(Peter MacCallum Cancer Centre)
- David G. Hunstman
(University of British Columbia)
- Sally M. Hunter
(Peter MacCallum Cancer Centre)
- Tom W. Jobling
(Monash Medical Centre)
- Kimberly R. Kalli
(Mayo Clinic)
- Scott H. Kaufmann
(Mayo Clinic)
- Catherine J. Kennedy
(University of Sydney)
- Martin Köbel
(The University of Calgary)
- Cecile Page
(CRCHUM)
- Jason Li
(Peter MacCallum Cancer Centre)
- Richard Lupat
(Peter MacCallum Cancer Centre)
- Orla M. McNally
(The University of Melbourne
Royal Womens Hospital)
- Jessica N. McAlpine
(University of British Columbia)
- Anne-Marie Mes-Masson
(CRCHUM
University of Montreal)
- Linda Mileshkin
(Peter MacCallum Cancer Centre)
- Diane M. Provencher
(CRCHUM
Centre Hospitalier de L’Université de Montreal)
- Jan Pyman
(Royal Womens Hospital
Royal Children’s Hospital)
- Kurosh Rahimi
(CRCHUM
Centre Hospitalier de L’Université de Montreal)
- Simone M. Rowley
(Peter MacCallum Cancer Centre)
- Carolina Salazar
(Peter MacCallum Cancer Centre)
- Goli Samimi
(Kinghorn Cancer Centre and Garvan Institute of Medical Research)
- Hugo Saunders
(Peter MacCallum Cancer Centre)
- Timothy Semple
(Peter MacCallum Cancer Centre)
- Ragwha Sharma
(University of Sydney
NSW Health Pathology)
- Alice J. Sharpe
(Monash University)
- Andrew N. Stephens
(Hudson Institute of Medical Research)
- Niko Thio
(Peter MacCallum Cancer Centre)
- Michelle C. Torres
(Peter MacCallum Cancer Centre)
- Nadia Traficante
(Peter MacCallum Cancer Centre
The University of Melbourne)
- Zhongyue Xing
(Peter MacCallum Cancer Centre)
- Magnus Zethoven
(Peter MacCallum Cancer Centre)
- Yoland C. Antill
(Cabrini Health
Frankston Hospital)
- Clare L. Scott
(Peter MacCallum Cancer Centre
Walter and Eliza Hall Institute
The University of Melbourne
Royal Melbourne Hospital)
- Ian G. Campbell
(Peter MacCallum Cancer Centre
The University of Melbourne)
- Kylie L. Gorringe
(Peter MacCallum Cancer Centre
The University of Melbourne)
Abstract
Mucinous ovarian carcinoma (MOC) is a unique subtype of ovarian cancer with an uncertain etiology, including whether it genuinely arises at the ovary or is metastatic disease from other organs. In addition, the molecular drivers of invasive progression, high-grade and metastatic disease are poorly defined. We perform genetic analysis of MOC across all histological grades, including benign and borderline mucinous ovarian tumors, and compare these to tumors from other potential extra-ovarian sites of origin. Here we show that MOC is distinct from tumors from other sites and supports a progressive model of evolution from borderline precursors to high-grade invasive MOC. Key drivers of progression identified are TP53 mutation and copy number aberrations, including a notable amplicon on 9p13. High copy number aberration burden is associated with worse prognosis in MOC. Our data conclusively demonstrate that MOC arise from benign and borderline precursors at the ovary and are not extra-ovarian metastases.
Suggested Citation
Dane Cheasley & Matthew J. Wakefield & Georgina L. Ryland & Prue E. Allan & Kathryn Alsop & Kaushalya C. Amarasinghe & Sumitra Ananda & Michael S. Anglesio & George Au-Yeung & Maret Böhm & David D. L., 2019.
"The molecular origin and taxonomy of mucinous ovarian carcinoma,"
Nature Communications, Nature, vol. 10(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11862-x
DOI: 10.1038/s41467-019-11862-x
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