Genes associated with progression and recurrence of hepatocellular carcinoma in hepatitis C patients waiting and undergoing liver transplantation: preliminary results
- PMID: 17460570
- DOI: 10.1097/01.tp.0000258643.05294.0b
Genes associated with progression and recurrence of hepatocellular carcinoma in hepatitis C patients waiting and undergoing liver transplantation: preliminary results
Abstract
Background: Liver transplantation (LT) represents a curative treatment for small hepatocellular carcinoma (HCC). Potentially curable higher-stage HCC patients are denied LT due to the lack of cancer markers that predict progression and recurrence.
Methods: Thirty-eight candidates for LT with hepatitis C virus (HCV) cirrhosis and HCC were studied. Gene expression (Gexp) analysis of tumor samples was performed using microarrays.
Results: Twenty patients underwent transplantation, 13 progressed while waiting for transplantation, 4 are alive awaiting transplantation, and 1 died without progression while waiting for LT. Differences in GExp among patients who underwent LT or did not progress (n=25) versus those whose disease progressed while waiting for LT (n=13) were assessed. Thus, 54 probe sets (Pset) were significantly differentially expressed. Among LT patients, 10 Psets were differentially expressed between LT patients with the same explanted stage that recurred (n=5) versus LT patients who did not recur (n=5). Ninety-eight Psets were significantly associated with survival at the alpha=0.005 level.
Conclusions: Here, we have identified genes associated with HCC progression in HCV-HCC patients awaiting LT transplantation. A limited number of genes were related to overall survival and cancer-free survival after LT. Incorporation of these molecular markers could help to improve organ allocation for HCV-HCC patients.
Similar articles
-
Hepatocellular carcinoma: Can it be considered a controversial indication for liver transplantation in centers with high rates of hepatitis C?Liver Transpl. 2002 Nov;8(11):1020-7. doi: 10.1053/jlts.2002.35664. Liver Transpl. 2002. PMID: 12424715
-
Liver resection for transplantable hepatocellular carcinoma: long-term survival and role of secondary liver transplantation.Ann Surg. 2009 Nov;250(5):738-46. doi: 10.1097/SLA.0b013e3181bd582b. Ann Surg. 2009. PMID: 19801927
-
HCV histological recurrence and survival following liver transplantation in patients with and without hepatocellular carcinoma.Transplant Proc. 2008 Jul-Aug;40(6):1974-5. doi: 10.1016/j.transproceed.2008.05.040. Transplant Proc. 2008. PMID: 18675104
-
[Liver transplantation for hepatocellular carcinoma].Korean J Hepatol. 2006 Dec;12(4):493-506. Korean J Hepatol. 2006. PMID: 17237627 Review. Korean.
-
Treatment before liver transplantation for HCC.Ann Surg Oncol. 2008 Apr;15(4):993-1000. doi: 10.1245/s10434-007-9787-8. Epub 2008 Jan 31. Ann Surg Oncol. 2008. PMID: 18236111 Review.
Cited by
-
Transcriptome analysis creates a new era of precision medicine for managing recurrent hepatocellular carcinoma.World J Gastroenterol. 2023 Feb 7;29(5):780-799. doi: 10.3748/wjg.v29.i5.780. World J Gastroenterol. 2023. PMID: 36816628 Free PMC article. Review.
-
KLHL21, a novel gene that contributes to the progression of hepatocellular carcinoma.BMC Cancer. 2016 Oct 21;16(1):815. doi: 10.1186/s12885-016-2851-7. BMC Cancer. 2016. PMID: 27769251 Free PMC article.
-
Liver Transplantation for Hepatocellular Carcinoma beyond Milan Criteria: Multidisciplinary Approach to Improve Outcome.ISRN Hepatol. 2014 Mar 4;2014:706945. doi: 10.1155/2014/706945. eCollection 2014. ISRN Hepatol. 2014. PMID: 27335840 Free PMC article. Review.
-
Deleted in liver cancer-1 (DLC1): an emerging metastasis suppressor gene.Mol Diagn Ther. 2014 Jun;18(3):293-302. doi: 10.1007/s40291-014-0086-3. Mol Diagn Ther. 2014. PMID: 24519699 Free PMC article. Review.
-
Multimodality therapy and liver transplantation for hepatocellular carcinoma: a 14-year prospective analysis of outcomes.Transplantation. 2014 Jul 15;98(1):100-6. doi: 10.1097/01.TP.0000441090.39840.b0. Transplantation. 2014. PMID: 24503764 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical