Patricia Taik

ORCID: 0000-0003-0990-7832
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About
Contact & Profiles
Research Areas
  • Liver Disease Diagnosis and Treatment
  • Hepatitis B Virus Studies
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Cancer Immunotherapy and Biomarkers
  • Bladder and Urothelial Cancer Treatments
  • Ubiquitin and proteasome pathways
  • Protist diversity and phylogeny
  • Renal cell carcinoma treatment
  • Soft tissue tumor case studies
  • Aquaculture disease management and microbiota
  • Urinary and Genital Oncology Studies
  • Adrenal and Paraganglionic Tumors
  • Pituitary Gland Disorders and Treatments
  • Genomics and Phylogenetic Studies
  • Chronic Lymphocytic Leukemia Research
  • Oral and Maxillofacial Pathology
  • Bone Tumor Diagnosis and Treatments
  • Hepatitis C virus research
  • Endoplasmic Reticulum Stress and Disease
  • Cancer Genomics and Diagnostics
  • Histone Deacetylase Inhibitors Research
  • Hormonal Regulation and Hypertension
  • Cancer, Lipids, and Metabolism
  • Cancer Treatment and Pharmacology
  • Colorectal Cancer Treatments and Studies

Sema4 (United States)
2019-2023

Icahn School of Medicine at Mount Sinai
2019-2021

Hamilton College
2017

Abstract Context Pituitary corticotroph adenomas are rare tumors that can be associated with excess adrenocorticotropin (ACTH) and adrenal cortisol production, resulting in the clinically debilitating endocrine condition Cushing disease. A subset of behave aggressively, genomic drivers behind development these largely unknown. Objective To investigate at risk for aggressive behavior. Design Whole-exome sequencing patient-matched tumor normal deoxyribonucleic acid (DNA) from a patient cohort...

10.1210/clinem/dgaa853 article EN The Journal of Clinical Endocrinology & Metabolism 2020-11-21

Adenoid cystic carcinoma (ACC) is a rare cancer type that originates in the salivary glands. Tumors commonly invade along nerve tracks head and neck, making surgery challenging. Follow-up treatments for recurrence or metastasis including chemotherapy targeted therapies have shown limited efficacy, emphasizing need new therapies. Here, we report Drosophila-based therapeutic approach patient with advanced ACC disease. A patient-specific Drosophila transgenic line was developed to model five...

10.1016/j.isci.2021.102212 article EN cc-by iScience 2021-02-21

Abstract Purpose: Mongolia has the world's highest incidence of hepatocellular carcinoma (HCC), with ∼100 cases/100,000 inhabitants, although reasons for this have not been thoroughly delineated. Experimental Design: We performed a molecular characterization Mongolian (n = 192) compared Western 187) HCCs by RNA sequencing and whole-exome to unveil distinct genomic transcriptomic features associated environmental factors in population. Results: patients were younger, higher female prevalence,...

10.1158/1078-0432.ccr-22-0632 article EN Clinical Cancer Research 2022-08-23

Abstract Ossifying fibromas are very rare tumors that sometimes seen as part of the hyperparathyroidism-jaw tumor syndrome (HPT-JT), which is caused by inactivating mutations HRPT2/CDC73 suppressor gene. CDC73 have been identified in a subset sporadic cases but aberrant expression encoded protein, parafibromin, has not demonstrated ossifying fibroma. We sought to determine if loss parafibromin regularly contributes development sporadic, nonsyndromic examined series 9 fibromas, including...

10.1210/jendso/bvab087 article EN Journal of the Endocrine Society 2021-05-08

Abstract Background Treatment options have been historically limited for cisplatin-ineligible patients with advanced urothelial carcinoma (UC). Given the need alternatives to platinum-based chemotherapy, including non-chemotherapy regimens both impaired renal function and borderline functional status, in 2010 (prior immune checkpoint blockade era metastatic UC), we initiated a phase II trial test activity of everolimus or plus paclitaxel setting. Methods This was an open-label conducted...

10.1093/oncolo/oyab075 article EN cc-by-nc The Oncologist 2022-01-26
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