Literature DB >> 30246169

Inference of Germline Mutational Status and Evaluation of Loss of Heterozygosity in High-Depth, Tumor-Only Sequencing Data.

Hossein Khiabanian1,2,3, Kim M Hirshfield1,4, Mendel Goldfinger1,4, Simon Bird2, Mark Stein1,4, Joseph Aisner1,4, Deborah Toppmeyer1,4, Serena Wong1,4, Nancy Chan1,4, Kalyani Dhar1, Jinesh Gheeya1, Hetal Vig1, Mohammad Hadigol1,2, Dean Pavlick5, Sepand Ansari2, Siraj Ali5, Bing Xia1,6, Lorna Rodriguez-Rodriguez1,7, Shridar Ganesan1,2,4.   

Abstract

PURPOSE: Inherited germline defects are implicated in up to 10% of human tumors, with particularly well-known roles in breast and ovarian cancers that harbor BRCA1/2-mutated genes. There is also increasing evidence for the role of germline alterations in other malignancies such as colon and pancreatic cancers. Mutations in familial cancer genes can be detected by high throughput sequencing (HTS), when applied to formalin-fixed paraffin-embedded (FFPE) tumor specimens. However, due to often lack of patient-matched control normal DNA and/or low tumor purity, there is limited ability to determine the genomic status of these alterations (germline versus somatic) and to assess the presence of loss of heterozygosity (LOH). These analyses, especially when applied to genes such as BRCA1/2, can have significant clinical implications for patient care.
METHODS: LOHGIC (LOH-Germline Inference Calculator) is a statistical model selection method to determine somatic-versus-germline status and predict LOH for mutations identified via clinical grade, high-depth, hybrid-capture tumor-only sequencing. LOHGIC incorporates statistical uncertainties inherent to HTS as well as specimen biases in tumor purity estimates, which we use to assess BRCA1/2 mutations in 1,636 specimens sequenced at Rutgers Cancer Institute of New Jersey.
RESULTS: Evaluation of LOHGIC with available germline sequencing from BRCA1/2 testing, demonstrates 93% accuracy, 100% precision, and 96% recall. This analysis highlights a differential tumor spectrum associated with BRCA1/2 mutations.
CONCLUSION: LOHGIC can assess LOH status for both germline and somatic mutations. It also can be applied to any gene with candidate, inherited mutations. This approach demonstrates the clinical utility of targeted sequencing in both identifying patients with potential germline alterations in tumor suppressor genes as well as estimating LOH occurrence in cancer cells, which may confer therapeutic relevance.

Entities:  

Year:  2018        PMID: 30246169      PMCID: PMC6148761          DOI: 10.1200/PO.17.00148

Source DB:  PubMed          Journal:  JCO Precis Oncol        ISSN: 2473-4284


  39 in total

Review 1.  BRCA1, PARP, and 53BP1: conditional synthetic lethality and synthetic viability.

Authors:  Amal Aly; Shridar Ganesan
Journal:  J Mol Cell Biol       Date:  2011-02       Impact factor: 6.216

2.  Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 Mutation.

Authors:  Amy Finch; Mario Beiner; Jan Lubinski; Henry T Lynch; Pal Moller; Barry Rosen; Joan Murphy; Parviz Ghadirian; Eitan Friedman; William D Foulkes; Charmaine Kim-Sing; Teresa Wagner; Nadine Tung; Fergus Couch; Dominique Stoppa-Lyonnet; Peter Ainsworth; Mary Daly; Babara Pasini; Ruth Gershoni-Baruch; Charis Eng; Olufunmilayo I Olopade; Jane McLennan; Beth Karlan; Jeffrey Weitzel; Ping Sun; Steven A Narod
Journal:  JAMA       Date:  2006-07-12       Impact factor: 56.272

3.  Two decades after BRCA: setting paradigms in personalized cancer care and prevention.

Authors:  Fergus J Couch; Katherine L Nathanson; Kenneth Offit
Journal:  Science       Date:  2014-03-28       Impact factor: 47.728

4.  Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE.

Authors:  Nasim Mavaddat; Susan Peock; Debra Frost; Steve Ellis; Radka Platte; Elena Fineberg; D Gareth Evans; Louise Izatt; Rosalind A Eeles; Julian Adlard; Rosemarie Davidson; Diana Eccles; Trevor Cole; Jackie Cook; Carole Brewer; Marc Tischkowitz; Fiona Douglas; Shirley Hodgson; Lisa Walker; Mary E Porteous; Patrick J Morrison; Lucy E Side; M John Kennedy; Catherine Houghton; Alan Donaldson; Mark T Rogers; Huw Dorkins; Zosia Miedzybrodzka; Helen Gregory; Jacqueline Eason; Julian Barwell; Emma McCann; Alex Murray; Antonis C Antoniou; Douglas F Easton
Journal:  J Natl Cancer Inst       Date:  2013-04-29       Impact factor: 13.506

Review 5.  Highly penetrant hereditary cancer syndromes.

Authors:  Rebecca Nagy; Kevin Sweet; Charis Eng
Journal:  Oncogene       Date:  2004-08-23       Impact factor: 9.867

6.  BRCA germline mutations in Jewish patients with pancreatic adenocarcinoma.

Authors:  Cristina R Ferrone; Douglas A Levine; Laura H Tang; Peter J Allen; William Jarnagin; Murray F Brennan; Kenneth Offit; Mark E Robson
Journal:  J Clin Oncol       Date:  2008-12-08       Impact factor: 44.544

Review 7.  BRCA1-hapoinsufficiency: Unraveling the molecular and cellular basis for tissue-specific cancer.

Authors:  Maja Sedic; Charlotte Kuperwasser
Journal:  Cell Cycle       Date:  2016       Impact factor: 4.534

8.  Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.

Authors:  Paolo Peterlongo; Jenny Chang-Claude; Kirsten B Moysich; Anja Rudolph; Rita K Schmutzler; Jacques Simard; Penny Soucy; Rosalind A Eeles; Douglas F Easton; Ute Hamann; Stefan Wilkening; Bowang Chen; Matti A Rookus; Marjanka K Schmidt; Frederieke H van der Baan; Amanda B Spurdle; Logan C Walker; Felicity Lose; Ana-Teresa Maia; Marco Montagna; Laura Matricardi; Jan Lubinski; Anna Jakubowska; Encarna B Gómez Garcia; Olufunmilayo I Olopade; Robert L Nussbaum; Katherine L Nathanson; Susan M Domchek; Timothy R Rebbeck; Banu K Arun; Beth Y Karlan; Sandra Orsulic; Jenny Lester; Wendy K Chung; Alex Miron; Melissa C Southey; David E Goldgar; Saundra S Buys; Ramunas Janavicius; Cecilia M Dorfling; Elizabeth J van Rensburg; Yuan Chun Ding; Susan L Neuhausen; Thomas V O Hansen; Anne-Marie Gerdes; Bent Ejlertsen; Lars Jønson; Ana Osorio; Cristina Martínez-Bouzas; Javier Benitez; Edye E Conway; Kathleen R Blazer; Jeffrey N Weitzel; Siranoush Manoukian; Bernard Peissel; Daniela Zaffaroni; Giulietta Scuvera; Monica Barile; Filomena Ficarazzi; Frederique Mariette; Stefano Fortuzzi; Alessandra Viel; Giuseppe Giannini; Laura Papi; Aline Martayan; Maria Grazia Tibiletti; Paolo Radice; Athanassios Vratimos; Florentia Fostira; Judy E Garber; Alan Donaldson; Carole Brewer; Claire Foo; D Gareth R Evans; Debra Frost; Diana Eccles; Angela Brady; Jackie Cook; Marc Tischkowitz; Julian Adlard; Julian Barwell; Lisa Walker; Louise Izatt; Lucy E Side; M John Kennedy; Mark T Rogers; Mary E Porteous; Patrick J Morrison; Radka Platte; Rosemarie Davidson; Shirley V Hodgson; Steve Ellis; Trevor Cole; Andrew K Godwin; Kathleen Claes; Tom Van Maerken; Alfons Meindl; Andrea Gehrig; Christian Sutter; Christoph Engel; Dieter Niederacher; Doris Steinemann; Hansjoerg Plendl; Karin Kast; Kerstin Rhiem; Nina Ditsch; Norbert Arnold; Raymonda Varon-Mateeva; Barbara Wappenschmidt; Shan Wang-Gohrke; Brigitte Bressac-de Paillerets; Bruno Buecher; Capucine Delnatte; Claude Houdayer; Dominique Stoppa-Lyonnet; Francesca Damiola; Isabelle Coupier; Laure Barjhoux; Laurence Venat-Bouvet; Lisa Golmard; Nadia Boutry-Kryza; Olga M Sinilnikova; Olivier Caron; Pascal Pujol; Sylvie Mazoyer; Muriel Belotti; Marion Piedmonte; Michael L Friedlander; Gustavo C Rodriguez; Larry J Copeland; Miguel de la Hoya; Pedro Perez Segura; Heli Nevanlinna; Kristiina Aittomäki; Theo A M van Os; Hanne E J Meijers-Heijboer; Annemarie H van der Hout; Maaike P G Vreeswijk; Nicoline Hoogerbrugge; Margreet G E M Ausems; Helena C van Doorn; J Margriet Collée; Edith Olah; Orland Diez; Ignacio Blanco; Conxi Lazaro; Joan Brunet; Lidia Feliubadalo; Cezary Cybulski; Jacek Gronwald; Katarzyna Durda; Katarzyna Jaworska-Bieniek; Grzegorz Sukiennicki; Adalgeir Arason; Jocelyne Chiquette; Manuel R Teixeira; Curtis Olswold; Fergus J Couch; Noralane M Lindor; Xianshu Wang; Csilla I Szabo; Kenneth Offit; Marina Corines; Lauren Jacobs; Mark E Robson; Liying Zhang; Vijai Joseph; Andreas Berger; Christian F Singer; Christine Rappaport; Daphne Geschwantler Kaulich; Georg Pfeiler; Muy-Kheng M Tea; Catherine M Phelan; Mark H Greene; Phuong L Mai; Gad Rennert; Anna Marie Mulligan; Gord Glendon; Sandrine Tchatchou; Irene L Andrulis; Amanda Ewart Toland; Anders Bojesen; Inge Sokilde Pedersen; Mads Thomassen; Uffe Birk Jensen; Yael Laitman; Johanna Rantala; Anna von Wachenfeldt; Hans Ehrencrona; Marie Stenmark Askmalm; Åke Borg; Karoline B Kuchenbaecker; Lesley McGuffog; Daniel Barrowdale; Sue Healey; Andrew Lee; Paul D P Pharoah; Georgia Chenevix-Trench; Antonis C Antoniou; Eitan Friedman
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2014-10-21       Impact factor: 4.254

9.  COSMIC: exploring the world's knowledge of somatic mutations in human cancer.

Authors:  Simon A Forbes; David Beare; Prasad Gunasekaran; Kenric Leung; Nidhi Bindal; Harry Boutselakis; Minjie Ding; Sally Bamford; Charlotte Cole; Sari Ward; Chai Yin Kok; Mingming Jia; Tisham De; Jon W Teague; Michael R Stratton; Ultan McDermott; Peter J Campbell
Journal:  Nucleic Acids Res       Date:  2014-10-29       Impact factor: 16.971

10.  ClinVar: public archive of relationships among sequence variation and human phenotype.

Authors:  Melissa J Landrum; Jennifer M Lee; George R Riley; Wonhee Jang; Wendy S Rubinstein; Deanna M Church; Donna R Maglott
Journal:  Nucleic Acids Res       Date:  2013-11-14       Impact factor: 16.971

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  7 in total

1.  Detection of Three Distinct Clonal Populations Using Circulating Cell Free DNA: A Cautionary Note on the Use of Liquid Biopsy.

Authors:  Gregory M Riedlinger; Nahed Jalloul; Elizabeth Poplin; Janice M Mehnert; Roman Groisberg; Hossein Khiabanian; Shridar Ganesan
Journal:  JCO Precis Oncol       Date:  2019-07-31

2.  All-FIT: allele-frequency-based imputation of tumor purity from high-depth sequencing data.

Authors:  Jui Wan Loh; Caitlin Guccione; Frances Di Clemente; Gregory Riedlinger; Shridar Ganesan; Hossein Khiabanian
Journal:  Bioinformatics       Date:  2020-04-01       Impact factor: 6.937

3.  Germline Testing for Patients With BRCA1/2 Mutations on Somatic Tumor Testing.

Authors:  Katherine Vlessis; Natasha Purington; Nicolette Chun; Sigurdis Haraldsdottir; James M Ford
Journal:  JNCI Cancer Spectr       Date:  2019-11-11

4.  Comprehensive molecular profiling of Taiwanese breast cancers revealed potential therapeutic targets: prevalence of actionable mutations among 380 targeted sequencing analyses.

Authors:  Chi-Cheng Huang; Yi-Fang Tsai; Chun-Yu Liu; Ta-Chung Chao; Pei-Ju Lien; Yen-Shu Lin; Chin-Jung Feng; Jen-Hwey Chiu; Chih-Yi Hsu; Ling-Ming Tseng
Journal:  BMC Cancer       Date:  2021-02-25       Impact factor: 4.430

5.  Germline Testing Data Validate Inferences of Mutational Status for Variants Detected From Tumor-Only Sequencing.

Authors:  Nahed Jalloul; Israel Gomy; Samantha Stokes; Alexander Gusev; Bruce E Johnson; Neal I Lindeman; Laura Macconaill; Shridar Ganesan; Judy E Garber; Hossein Khiabanian
Journal:  JCO Precis Oncol       Date:  2021-11-17

6.  RET rearrangements are actionable alterations in breast cancer.

Authors:  Bhavna S Paratala; Jon H Chung; Casey B Williams; Bahar Yilmazel; Whitney Petrosky; Kirstin Williams; Alexa B Schrock; Laurie M Gay; Ellen Lee; Sonia C Dolfi; Kien Pham; Stephanie Lin; Ming Yao; Atul Kulkarni; Frances DiClemente; Chen Liu; Lorna Rodriguez-Rodriguez; Shridar Ganesan; Jeffrey S Ross; Siraj M Ali; Brian Leyland-Jones; Kim M Hirshfield
Journal:  Nat Commun       Date:  2018-11-16       Impact factor: 14.919

7.  Clonal Evolution of TP53 c.375+1G>A Mutation in Pre- and Post- Neo-Adjuvant Chemotherapy (NACT) Tumor Samples in High-Grade Serous Ovarian Cancer (HGSOC).

Authors:  Marica Garziera; Erika Cecchin; Giorgio Giorda; Roberto Sorio; Simona Scalone; Elena De Mattia; Rossana Roncato; Sara Gagno; Elena Poletto; Loredana Romanato; Fabrizio Ecca; Vincenzo Canzonieri; Giuseppe Toffoli
Journal:  Cells       Date:  2019-10-01       Impact factor: 6.600

  7 in total

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