Pathognomonic genetic signatures of gallbladder cancer: Results of ongoing prospective study.

e16236 Background: Gene polymorphisms play a pivotal role in gallbladder cancer (GBC) susceptibility and progression, underscoring the need to pinpoint key variants for enhanced diagnostic and therapeutic strategies. Methods: We performed germline and somatic whole exome sequencing (WES) of gallbladder cancer patients. WES was done by TarGT Absolute (4BASECARE) under armed forces medical research project. Patient recruitment was done after ethics committee approval. Results: 26 patients were enrolled from Jan 2021 till Dec 2023. Table depicts the baseline demographics. A total of 10 single nucleotide polymorphisms (SNPs) spanning nine candidate genes— XRCC1, CR1, APOB, CYP1B1, NAT2, ERCC2, OGG1, GSTP1 , and XPC —were prioritized based on their established or putative roles in DNA repair, xenobiotic metabolism, lipid regulation, and immune complex clearance. Notable findings include significant associations of GSTP1 (rs1138272) and CR1 (rs17259045) variants with elevated GBC risk, implicating impaired detoxification pathways and reduced immune complex clearance as contributors to tumorigenesis. Additionally, 9% of the patient cohort presented with pathogenic mutations in ATM, BRCA1, FANCC genes indicating elevated risk of cancer in these patients as compared to the normal population. We also observed deleterious mutations in six genes FREM1, MYO3A, ZFHX3, RAX2, ASPM, and NANOS1 in the cohort. Conclusions: By integrating germline whole-exome sequencing we have identified potential genetic variants and implicated genes that may contribute to GBC tumor formation. These findings provide a foundation for future research and explore their clinical utility in improving early detection and therapeutic approaches for GBC. Baseline demographic characteristics of study participants (n=26). Variables Frequency n (%) Age years Median Range 31-77 <=50 years 6 (23) >50 years 20 (77) Gender Female 17 (65) Male 9 (35) Cholelithiasis No 14 (54) Yes 12 (46) Cholecystectomy Not done 18 (70) Done 8 (30) Gangetic Belt Residence Yes 14 (54) No 12 (46) Jaundice on presentation Absent 14 (54) Present 12 (46) Bilirubin <=4 mg/dl 19 (73) >4 mg/dl 7 (23)

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Publication Details

Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.e16236
Primary Topic
Cholangiocarcinoma and Gallbladder Cancer Studies
Type
article
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0.00
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article

Pathognomonic genetic signatures of gallbladder cancer: Results of ongoing prospective study.

M. R. Kaushik, Satya Prakash Khuntia, Amol Patel, Vidya Veldore et al.
Journal of Clinical Oncology
Cholangiocarcinoma and Gallbladder Cancer Studies
article

Pathognomonic genetic signatures of gallbladder cancer: Results of ongoing prospective study.

M. R. Kaushik, Satya Prakash Khuntia, Amol Patel, Vidya Veldore, Arti Sarin, Nilesh Mukherjee, J Vyomesh, Kiran Kumar Ponugumati
article en

Abstract

e16236 Background: Gene polymorphisms play a pivotal role in gallbladder cancer (GBC) susceptibility and progression, underscoring the need to pinpoint key variants for enhanced diagnostic and therapeutic strategies. Methods: We performed germline and somatic whole exome sequencing (WES) of gallbladder cancer patients. WES was done by TarGT Absolute (4BASECARE) under armed forces medical research project. Patient recruitment was done after ethics committee approval. Results: 26 patients were enrolled from Jan 2021 till Dec 2023. Table depicts the baseline demographics. A total of 10 single nucleotide polymorphisms (SNPs) spanning nine candidate genes— XRCC1, CR1, APOB, CYP1B1, NAT2, ERCC2, OGG1, GSTP1 , and XPC —were prioritized based on their established or putative roles in DNA repair, xenobiotic metabolism, lipid regulation, and immune complex clearance. Notable findings include significant associations of GSTP1 (rs1138272) and CR1 (rs17259045) variants with elevated GBC risk, implicating impaired detoxification pathways and reduced immune complex clearance as contributors to tumorigenesis. Additionally, 9% of the patient cohort presented with pathogenic mutations in ATM, BRCA1, FANCC genes indicating elevated risk of cancer in these patients as compared to the normal population. We also observed deleterious mutations in six genes FREM1, MYO3A, ZFHX3, RAX2, ASPM, and NANOS1 in the cohort. Conclusions: By integrating germline whole-exome sequencing we have identified potential genetic variants and implicated genes that may contribute to GBC tumor formation. These findings provide a foundation for future research and explore their clinical utility in improving early detection and therapeutic approaches for GBC. Baseline demographic characteristics of study participants (n=26). Variables Frequency n (%) Age years Median Range 31-77 <=50 years 6 (23) >50 years 20 (77) Gender Female 17 (65) Male 9 (35) Cholelithiasis No 14 (54) Yes 12 (46) Cholecystectomy Not done 18 (70) Done 8 (30) Gangetic Belt Residence Yes 14 (54) No 12 (46) Jaundice on presentation Absent 14 (54) Present 12 (46) Bilirubin <=4 mg/dl 19 (73) >4 mg/dl 7 (23)

Journal of Clinical OncologyVol. 43(16_suppl)
Government of India (IN), INHS Asvini (IN), Command Hospital (IN)
Openalex Percentile: Top 79%
Cholangiocarcinoma and Gallbladder Cancer Studies
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