GALNT14 genotype effectively predicts the therapeutic response in unresectable hepatocellular carcinoma treated with transcatheter arterial chemoembolization

Kung Hao Liang, Chih Lang Lin, Sung Fang Chen, Chih Wei Chiu, Pei Ching Yang, Ming Ling Chang, Chen Chun Lin, Kai Feng Sung, Cassandra Yeh, Chien Fu Hung, Rong Nan Chien, Chau Ting Yeh*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)

Abstract

Aim: Transcatheter arterial chemoembolization is currently the standard treatment in hepatocellular carcinoma patients with Barcelona Clinic Liver Cancer stage B. Genomic variants of GALNT14 were recently identified as effective predictors for chemotherapy responses in Barcelona Clinic Liver Cancer stage C patients. Methods: We investigated the prognosis predictive value of GALNT14 genotypes in 327 hepatocelluar carcinoma patients treated by transcatheter arterial chemoembolization. Result: Cox proportional hazards model analysis showed that the genotype 'TT' was associated with shorter time-to-response (multivariate p < 0.001), time-to-complete-response (p = 0.004) and longer time-to-tumor progression (p < 0.001), compared with the genotype 'non-TT'. In patients with albumin <3.5 g/dl, genotype 'TT' was associated with longer overall survival (p = 0.027). Finally, genotype 'TT' correlated with higher cancer-to-noncancer ratios of GALNT14 protein levels, lower cancer-to-noncancer ratios of antiapoptotic cFLIP-S, and a clustered glycosylation pattern in the extracellular domain of death receptor 5. Conclusion: GALNT14 genotypes were significantly associated with clinical outcomes of transcatheter arterial chemoembolization. The differential status of extrinsic apoptotic signaling between cancerous and non-cancerous tissues might underlie the clinical association.

Original languageEnglish
Pages (from-to)353-366
Number of pages14
JournalPharmacogenomics
Volume17
Issue number4
DOIs
Publication statusPublished - 2016 Mar

Keywords

  • O-glycosylation
  • apoptosis
  • death receptor
  • sorafenib

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics
  • Pharmacology

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