Sheron Perera

ORCID: 0000-0001-8048-0611
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About
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Research Areas
  • Cancer Genomics and Diagnostics
  • Pancreatic and Hepatic Oncology Research
  • Genetic factors in colorectal cancer
  • Renal cell carcinoma treatment
  • DNA Repair Mechanisms
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Neuroendocrine Tumor Research Advances
  • Colorectal Cancer Treatments and Studies
  • Epigenetics and DNA Methylation
  • Adenosine and Purinergic Signaling
  • RNA and protein synthesis mechanisms
  • Diverticular Disease and Complications
  • Cell Adhesion Molecules Research
  • PI3K/AKT/mTOR signaling in cancer
  • Esophageal Cancer Research and Treatment
  • Melanoma and MAPK Pathways
  • BRCA gene mutations in cancer
  • Protein Kinase Regulation and GTPase Signaling
  • Gastrointestinal disorders and treatments
  • Innovations in Medical Education
  • Liver physiology and pathology
  • Esophageal and GI Pathology
  • Hepatitis B Virus Studies
  • Caveolin-1 and cellular processes
  • Organ Transplantation Techniques and Outcomes

University of Toronto
2005-2024

Sunnybrook Health Science Centre
2023-2024

Memorial Sloan Kettering Cancer Center
2024

Medical College of Wisconsin
2024

Princess Margaret Cancer Centre
2020-2023

University Health Network
2020-2022

Western University
2018

London Health Sciences Centre
2018

Lunenfeld-Tanenbaum Research Institute
2006-2010

Mount Sinai Hospital
2006-2010

Modified FOLFIRINOX (mFFX) and gemcitabine/nab-paclitaxel (GnP) remain standard first-line options for patients with advanced pancreatic ductal adenocarcinoma (PDAC). Human equilibrative nucleoside transporter 1 (hENT1) was hypothesized to be a biomarker of gemcitabine in the adjuvant setting, conflicting results. In this study, we explore hENT1 mRNA expression as predictive PDAC.COMPASS prospective observational trial PDAC. A biopsy required prior initiating chemotherapy, determined by...

10.1158/1078-0432.ccr-22-2576 article EN Clinical Cancer Research 2022-10-12

Epidermal growth factor receptor (EGFR) T790M mutations can be detected in the circulating tumour DNA from plasma of patients with non-small cell lung cancer (NSCLC) to triage for osimertinib eligibility and monitor longitudinally development T790M-mediated resistance.Using droplet digital PCR (ddPCR), we examined EGFR status 343 sequential NSCLC correlated mutational demographic clinical features. Where available, serial blood test results were assessed identify triggers timing repeat...

10.1136/jclinpath-2020-206668 article EN cc-by-nc Journal of Clinical Pathology 2020-05-29

Germline mutations in the mismatch repair genes lead to Lynch syndrome/ HNPCC, and genetic testing is offered identify individuals at risk of developing this disease. About a third all alterations detected gene MutL homolog 1 (MLH1) are missense variants. The majority these variants equivocal clinical significance. In report, we investigate molecular basis pathogenicity three localized distinct functional domains. Our results demonstrate that MLH1 p.Arg265Cys (c.793C>T) p.Lys618Ala...

10.1002/humu.9523 article EN Human Mutation 2008-01-18

Hepatocellular carcinoma (HCC) recurs after liver transplantation (LT) in ~17% of patients. We aimed to retrospectively compare the outcomes patients treated with different tyrosine kinase inhibitors (TKIs) for recurrent HCC post-LT.

10.1097/tp.0000000000005240 article EN Transplantation 2024-11-06

Gender equity has historically been a challenge within gastroenterology.The Canadian Association of Gastroenterology (CAG) developed survey to identify issues pertaining and gender faced by its membership determine areas action.In 2014, the was emailed all 1155 CAG members, data were analyzed using statistical methods.One hundred eleven members responded survey. Of those, 52% male, 75% between 26 45 years age, 55% in their first decade practice. More males held status full professor (21%...

10.1093/jcag/gwy044 article EN cc-by-nc Journal of the Canadian Association of Gastroenterology 2018-07-22

10.4267/2042/38427 article EN Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011-02-01

We would like to thank Boyd and colleagues for their thoughtful comments on our work demonstrating hENT1 as a predictive biomarker gemcitabine nab-paclitaxel (GnP) in advanced pancreatic ductal carcinoma (PDAC) the COMPASS trial (NCT02750657; ref. 1). These findings will be further validated ongoing phase II PASS-01 (ref. 2; NCT04469556), randomizing patients either modified FOLFIRINOX (mFFX) or GnP.The authors correctly highlight RNA expression after laser capture microdissection (LCM)...

10.1158/1078-0432.ccr-23-0887 article EN Clinical Cancer Research 2023-08-01

<div>AbstractPurpose:<p>Modified FOLFIRINOX (mFFX) and gemcitabine/nab-paclitaxel (GnP) remain standard first-line options for patients with advanced pancreatic ductal adenocarcinoma (PDAC). Human equilibrative nucleoside transporter 1 (hENT1) was hypothesized to be a biomarker of gemcitabine in the adjuvant setting, conflicting results. In this study, we explore hENT1 mRNA expression as predictive PDAC.</p>Experimental Design:<p>COMPASS prospective observational...

10.1158/1078-0432.c.6532926 preprint EN 2023-04-01

4011 Background: Human equilibrative nucleoside transporter 1 (hENT1) belongs to a family of transporters critical entry gemcitabine into cells. The prognostic and predictive characteristics this biomarker in pancreatic ductal adenocarcinoma (PDAC) have primarily been evaluated by immunohistochemistry, with conflicting results. We explored the impact hENT1 gene expression Comprehensive Molecular Characterization Advanced Ductal Pancreas Adenocarcinoma for Better Treatment Selection (COMPASS)...

10.1200/jco.2021.39.15_suppl.4011 article EN Journal of Clinical Oncology 2021-05-20

430 Background: Familial pancreatic cancer (FPC) is broadly defined as kindreds with at least a pair of first-degree relatives ductal adenocarcinoma (PDA). The role DNA damage response agents, including platinum has not been well studied in this patient population. Methods: In retrospective analysis, treatment details and clinical outcomes were analyzed pts FPC advanced, unresectable or recurrent disease enrolled the Ontario Pancreatic Cancer Study database. primary outcome, overall survival...

10.1200/jco.2021.39.3_suppl.430 article EN Journal of Clinical Oncology 2021-01-20

396 Background: BRCA1/2 and PALB2 are genes critical to the faithful repair of double strand breaks through homologous recombination (HRR) pathway. Alterations in these serve as predictive biomarkers both platinum PARP inhibitors. Ataxia-telangiectasia mutated ( ATM) is also indirectly involved HRR; however, its role a biomarker DNA damage response agents debated. Herein we evaluated genomic characteristics clinical outcomes patients with ATM alterations on Comprehensive Molecular...

10.1200/jco.2021.39.3_suppl.396 article EN Journal of Clinical Oncology 2021-01-20

Review on STK11 (serine/threonine kinase 11), with data DNA, the protein encoded, and where gene is implicated.

10.4267/2042/38417 article EN Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011-02-01

<div>AbstractPurpose:<p>Modified FOLFIRINOX (mFFX) and gemcitabine/nab-paclitaxel (GnP) remain standard first-line options for patients with advanced pancreatic ductal adenocarcinoma (PDAC). Human equilibrative nucleoside transporter 1 (hENT1) was hypothesized to be a biomarker of gemcitabine in the adjuvant setting, conflicting results. In this study, we explore hENT1 mRNA expression as predictive PDAC.</p>Experimental Design:<p>COMPASS prospective observational...

10.1158/1078-0432.c.6532926.v1 preprint EN 2023-04-01
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