TY - JOUR
T1 - Bioplatforms in liquid biopsy
T2 - advances in the techniques for isolation, characterization and clinical applications
AU - Shah, Ushma Jaykamal
AU - Alsulimani, Ahmad
AU - Ahmad, Faraz
AU - Mathkor, Darin Mansor
AU - Alsaieedi, Ahdab
AU - Harakeh, Steve
AU - Nasiruddin, Mohammad
AU - Haque, Shafiul
N1 - Publisher Copyright:
© 2022 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Tissue biopsy analysis has conventionally been the gold standard for cancer prognosis, diagnosis and prediction of responses/resistances to treatments. The existing biopsy procedures used in clinical practice are, however, invasive, painful and often associated with pitfalls like poor recovery of tumor cells and infeasibility for repetition in single patients. To circumvent these limitations, alternative non-invasive, rapid and economical, yet sturdy, consistent and dependable, biopsy techniques are required. Liquid biopsy is an emerging technology that fulfills these criteria and potentially much more in terms of subject-specific real-time monitoring of cancer progression, determination of tumor heterogeneity and treatment responses, and specific identification of the type and stages of cancers. The present review first briefly revisits the state-of-the-art technique of liquid biopsy and then proceeds to address in detail, the advances in the potential clinical applications of four major biological agencies present in liquid biopsy samples (circulating tumor DNA (ctDNA), circulating tumor cells (CTCs), exosomes and tumor-educated platelets (TEPs)). Finally, the authors conclude with the limitations that need to be addressed in order for liquid biopsy to effectively replace the conventional invasive biopsy methods in the clinical settings.
AB - Tissue biopsy analysis has conventionally been the gold standard for cancer prognosis, diagnosis and prediction of responses/resistances to treatments. The existing biopsy procedures used in clinical practice are, however, invasive, painful and often associated with pitfalls like poor recovery of tumor cells and infeasibility for repetition in single patients. To circumvent these limitations, alternative non-invasive, rapid and economical, yet sturdy, consistent and dependable, biopsy techniques are required. Liquid biopsy is an emerging technology that fulfills these criteria and potentially much more in terms of subject-specific real-time monitoring of cancer progression, determination of tumor heterogeneity and treatment responses, and specific identification of the type and stages of cancers. The present review first briefly revisits the state-of-the-art technique of liquid biopsy and then proceeds to address in detail, the advances in the potential clinical applications of four major biological agencies present in liquid biopsy samples (circulating tumor DNA (ctDNA), circulating tumor cells (CTCs), exosomes and tumor-educated platelets (TEPs)). Finally, the authors conclude with the limitations that need to be addressed in order for liquid biopsy to effectively replace the conventional invasive biopsy methods in the clinical settings.
KW - Liquid biopsy
KW - cell-free DNA (cfDNA)
KW - circulating tumor DNA (ctDNA)
KW - circulating tumor cells (CTCs)
KW - exosomes
KW - tumor-educated platelets (TEPs)
UR - https://www.scopus.com/pages/publications/85135905051
U2 - 10.1080/02648725.2022.2108994
DO - 10.1080/02648725.2022.2108994
M3 - Artículo de revisión
C2 - 35968863
AN - SCOPUS:85135905051
SN - 0264-8725
VL - 38
SP - 339
EP - 383
JO - Biotechnology and Genetic Engineering Reviews
JF - Biotechnology and Genetic Engineering Reviews
IS - 2
ER -