Blood-derived lncRNAs as potential biomarkers for early cancer diagnosis: The Good, the Bad and the Beauty

TL;DR

This review discusses the potential of circulating long non-coding RNAs (lncRNAs) in blood as early cancer biomarkers, highlighting progress, challenges, and future clinical applications for improved diagnosis and therapy.

Contribution

It provides a comprehensive overview of the current state, challenges, and clinical prospects of blood-derived lncRNAs as cancer biomarkers, including methodological recommendations.

Findings

Circulating lncRNAs show promise as early cancer biomarkers.

Specificity and sensitivity issues remain challenges.

Potential for therapeutic targeting and prognostic use.

Abstract

Cancer ranks as one of the deadliest diseases worldwide. The high mortality rate associated with cancer is partially due to the lack of reliable early detection methods and/or inaccurate diagnostic tools such as certain protein biomarkers. Cell-free nucleic acids (cfNA) such as circulating long non-coding RNAs (lncRNAs) have recently been proposed as a new class of potential biomarkers that could improve cancer diagnosis. The reported correlation between circulating lncRNA levels and the presence of tumors has triggered a great amount of interest among clinicians and scientists who have been actively investigating their potentials as reliable cancer biomarkers. In this report, we review the progress achieved (the Good) and challenges encountered (the Bad) in the development of circulating lncRNAs as potential biomarkers for early cancer diagnosis. We report and discuss the specificity and sensitivity issues of blood-based lncRNAs currently considered as promising biomarkers for various cancers such as hepatocellular carcinoma, colorectal cancer, gastric cancer and prostate cancer. We also emphasize the potential clinical applications (the Beauty) of circulating lncRNAs both as therapeutic targets and agents, on top of diagnostic and prognostic capabilities. Based on different published works, we finally provide recommendations for investigators who seek to investigate and compare the levels of circulating lncRNAs in the blood of cancer patients compared to healthy subjects by RT-qPCR or Next Generation Sequencing.