Cancer biomarkers for targeted therapy

Abstract Tumor-associated antigens (TAA) or cancer biomarkers are major targets for cancer therapies. Antibody- based agents targeting the cancer biomarkers include monoclonal antibodies (MoAbs), radiolabeled MoAbs, bispecific T cell engagers, and antibody-drug conjugates. Antibodies targeting CD19,...

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Main Author: Delong Liu
Format: Article
Language:English
Published: BMC 2019-11-01
Series:Biomarker Research
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40364-019-0178-7
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spelling doaj-45373372a6e14564adeffe363c8b8df62020-11-25T04:00:55ZengBMCBiomarker Research2050-77712019-11-01711710.1186/s40364-019-0178-7Cancer biomarkers for targeted therapyDelong Liu0New York Medical CollegeAbstract Tumor-associated antigens (TAA) or cancer biomarkers are major targets for cancer therapies. Antibody- based agents targeting the cancer biomarkers include monoclonal antibodies (MoAbs), radiolabeled MoAbs, bispecific T cell engagers, and antibody-drug conjugates. Antibodies targeting CD19, CD20, CD22, CD30, CD33, CD38, CD79B and SLAMF7 are in clinical applications for hematological malignancies. CD123, CLL-1, B cell maturation antigen, and CD138 are targets for cancer immunotherapeutic agents, including the chimeric antigen receptor - engineered T cells. Immune checkpoint inhibitors (ICIs) against PD-1, PD-L1, and CTLA-4 have led to the revolution of cancer immunotherapy. More ICIs targeting IDO, LAG3, TIM-3, TIGIT, SIGLECs, VISTA and CD47 are being explored. Small molecule inhibitors (SMIs) against tyrosine kinase oncoproteins such as BCR-ABL, JAK2, Bruton tyrosine kinase, FLT3, EGFR, ALK, HER2, VEGFR, FGFR, MEK, and MET have fundamentally changed the landscape of cancer therapy. SMIs against BCL-2, IDHs, BRAF, PI3 kinase, mTOR, PARP, and CDKs have become the mainstay in the treatment of a variety of cancer types. To reduce and avoid off-tumor toxicities, cancer-specific TAAs such as CD33 are being manufactured through systems biology approach. Search for novel biomarkers and new designs as well as delivery methods of targeted agents are fueling the next wave of advances in cancer therapy.http://link.springer.com/article/10.1186/s40364-019-0178-7BiomarkerTumor-associated antigenBiTEAntibody-drug conjugateCAR-T
collection DOAJ
language English
format Article
sources DOAJ
author Delong Liu
spellingShingle Delong Liu
Cancer biomarkers for targeted therapy
Biomarker Research
Biomarker
Tumor-associated antigen
BiTE
Antibody-drug conjugate
CAR-T
author_facet Delong Liu
author_sort Delong Liu
title Cancer biomarkers for targeted therapy
title_short Cancer biomarkers for targeted therapy
title_full Cancer biomarkers for targeted therapy
title_fullStr Cancer biomarkers for targeted therapy
title_full_unstemmed Cancer biomarkers for targeted therapy
title_sort cancer biomarkers for targeted therapy
publisher BMC
series Biomarker Research
issn 2050-7771
publishDate 2019-11-01
description Abstract Tumor-associated antigens (TAA) or cancer biomarkers are major targets for cancer therapies. Antibody- based agents targeting the cancer biomarkers include monoclonal antibodies (MoAbs), radiolabeled MoAbs, bispecific T cell engagers, and antibody-drug conjugates. Antibodies targeting CD19, CD20, CD22, CD30, CD33, CD38, CD79B and SLAMF7 are in clinical applications for hematological malignancies. CD123, CLL-1, B cell maturation antigen, and CD138 are targets for cancer immunotherapeutic agents, including the chimeric antigen receptor - engineered T cells. Immune checkpoint inhibitors (ICIs) against PD-1, PD-L1, and CTLA-4 have led to the revolution of cancer immunotherapy. More ICIs targeting IDO, LAG3, TIM-3, TIGIT, SIGLECs, VISTA and CD47 are being explored. Small molecule inhibitors (SMIs) against tyrosine kinase oncoproteins such as BCR-ABL, JAK2, Bruton tyrosine kinase, FLT3, EGFR, ALK, HER2, VEGFR, FGFR, MEK, and MET have fundamentally changed the landscape of cancer therapy. SMIs against BCL-2, IDHs, BRAF, PI3 kinase, mTOR, PARP, and CDKs have become the mainstay in the treatment of a variety of cancer types. To reduce and avoid off-tumor toxicities, cancer-specific TAAs such as CD33 are being manufactured through systems biology approach. Search for novel biomarkers and new designs as well as delivery methods of targeted agents are fueling the next wave of advances in cancer therapy.
topic Biomarker
Tumor-associated antigen
BiTE
Antibody-drug conjugate
CAR-T
url http://link.springer.com/article/10.1186/s40364-019-0178-7
work_keys_str_mv AT delongliu cancerbiomarkersfortargetedtherapy
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