» Articles » PMID: 31001651

Random Gene Sets in Predicting Survival of Patients with Hepatocellular Carcinoma

Overview
Specialty General Medicine
Date 2019 Apr 20
PMID 31001651
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Despite multiple publications, molecular signatures predicting the course of hepatocellular carcinoma (HCC) have not yet been integrated into clinical routine decision-making. Given the diversity of published signatures, optimal number, best combinations, and benefit of functional associations of genes in prognostic signatures remain to be defined. We investigated a vast number of randomly chosen gene sets (varying between 1 and 10,000 genes) to encompass the full range of prognostic gene sets on 242 transcriptomic profiles of patients with HCC. Depending on the selected size, 4.7 to 23.5% of all random gene sets exhibit prognostic potential by separating patient subgroups with significantly diverse survival. This was further substantiated by investigating gene sets and signaling pathways also resulting in a comparable high number of significantly prognostic gene sets. However, combining multiple random gene sets using "swarm intelligence" resulted in a significantly improved predictability for approximately 63% of all patients. In these patients, approx. 70% of all random 50-gene containing gene sets resulted in equal and stable prediction of survival. For all other patients, a reliable prediction seems highly unlikely for any selected gene set. Using a machine learning and independent validation approach, we demonstrated a high reliability of random gene sets and swarm intelligence in HCC prognosis. Ultimately, these findings were validated in two independent patient cohorts and independent technical platforms (microarray, RNASeq). In conclusion, we demonstrate that using "swarm intelligence" of multiple gene sets for prognosis prediction may not only be superior but also more robust for predictive purposes. KEY MESSAGES: Molecular signatures predicting HCC have not yet been integrated into clinical routine Depending on the selected size, 4.7 to 23.5% of all random gene sets exhibit prognostic potential; independent of the technical platform (microarray, RNASeq) Using "swarm intelligence" resulted in a significantly improved predictability In these patients, approx. 70% of all random 50-gene containing gene sets resulted in equal and stable prediction of survival Overall, "swarm intelligence" is superior and more robust for predictive purposes in HCC.

Citing Articles

Artificial intelligence in the detection, characterisation and prediction of hepatocellular carcinoma: a narrative review.

Kawka M, Dawidziuk A, Jiao L, Gall T Transl Gastroenterol Hepatol. 2022; 7:41.

PMID: 36300146 PMC: 9468986. DOI: 10.21037/tgh-20-242.


Deep View of HCC Gene Expression Signatures and Their Comparison with Other Cancers.

Qian Y, Itzel T, Ebert M, Teufel A Cancers (Basel). 2022; 14(17).

PMID: 36077860 PMC: 9454845. DOI: 10.3390/cancers14174322.


Associating Preoperative MRI Features and Gene Expression Signatures of Early-stage Hepatocellular Carcinoma Patients using Machine Learning.

Li X, Cheng L, Li C, Hu X, Hu X, Tan L J Clin Transl Hepatol. 2022; 10(1):63-71.

PMID: 35233374 PMC: 8845145. DOI: 10.14218/JCTH.2021.00023.


Identification of Immune-Related LncRNA Pairs for Predicting Prognosis and Immunotherapeutic Response in Head and Neck Squamous Cell Carcinoma.

Wang X, Cao K, Guo E, Mao X, Guo L, Zhang C Front Immunol. 2021; 12:658631.

PMID: 33995377 PMC: 8116744. DOI: 10.3389/fimmu.2021.658631.


Identification of an IRGP Signature to Predict Prognosis and Immunotherapeutic Efficiency in Bladder Cancer.

Zhang L, Li L, Zhan Y, Zhu Z, Zhang X Front Mol Biosci. 2021; 8:607090.

PMID: 33937319 PMC: 8082411. DOI: 10.3389/fmolb.2021.607090.


References
1.
Itzel T, Scholz P, Maass T, Krupp M, Marquardt J, Strand S . Translating bioinformatics in oncology: guilt-by-profiling analysis and identification of KIF18B and CDCA3 as novel driver genes in carcinogenesis. Bioinformatics. 2014; 31(2):216-24. PMC: 4287940. DOI: 10.1093/bioinformatics/btu586. View

2.
Lee J, Heo J, Libbrecht L, Chu I, Kaposi-Novak P, Calvisi D . A novel prognostic subtype of human hepatocellular carcinoma derived from hepatic progenitor cells. Nat Med. 2006; 12(4):410-6. DOI: 10.1038/nm1377. View

3.
Gerlinger M, Rowan A, Horswell S, Math M, Larkin J, Endesfelder D . Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med. 2012; 366(10):883-892. PMC: 4878653. DOI: 10.1056/NEJMoa1113205. View

4.
Ioannidis J . Expectations, validity, and reality in omics. J Clin Epidemiol. 2010; 63(9):945-9. DOI: 10.1016/j.jclinepi.2010.04.002. View

5.
Wooden B, Goossens N, Hoshida Y, Friedman S . Using Big Data to Discover Diagnostics and Therapeutics for Gastrointestinal and Liver Diseases. Gastroenterology. 2016; 152(1):53-67.e3. PMC: 5193106. DOI: 10.1053/j.gastro.2016.09.065. View