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,...
Main Author: | |
---|---|
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 |
id |
doaj-45373372a6e14564adeffe363c8b8df6 |
---|---|
record_format |
Article |
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 |
_version_ |
1724448499394674688 |