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The effects of T-DXd on the expression of HLA class I and chemokines CXCL9/10/11 in HER2-overexpressing gastric cancer cells
by
Mimura, Kosaku
, Watanabe, Yohei
, Saito, Motonobu
, Matsumoto, Takuro
, Neupane, Prajwal
, Thar Min, Aung Kyi
, Hanayama, Hiroyuki
, Ito, Misato
, Okayama, Hirokazu
, Kanke, Yasuyuki
, Nakajima, Shotaro
, Hayase, Suguru
, Saze, Zenichiro
, Nakano, Hiroshi
, Momma, Tomoyuki
, Kono, Koji
in
631/250/580
/ 631/67/1504
/ CD8 antigen
/ Cell proliferation
/ Chemokines
/ Chemotactic factors
/ DNA damage
/ DNA topoisomerase
/ ErbB-2 protein
/ Gastric cancer
/ Gene expression
/ Histocompatibility antigen HLA
/ Humanities and Social Sciences
/ Lymphocytes T
/ Monoclonal antibodies
/ multidisciplinary
/ Science
/ Science (multidisciplinary)
/ Trastuzumab
/ Tumor cells
/ Tumors
2021
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The effects of T-DXd on the expression of HLA class I and chemokines CXCL9/10/11 in HER2-overexpressing gastric cancer cells
by
Mimura, Kosaku
, Watanabe, Yohei
, Saito, Motonobu
, Matsumoto, Takuro
, Neupane, Prajwal
, Thar Min, Aung Kyi
, Hanayama, Hiroyuki
, Ito, Misato
, Okayama, Hirokazu
, Kanke, Yasuyuki
, Nakajima, Shotaro
, Hayase, Suguru
, Saze, Zenichiro
, Nakano, Hiroshi
, Momma, Tomoyuki
, Kono, Koji
in
631/250/580
/ 631/67/1504
/ CD8 antigen
/ Cell proliferation
/ Chemokines
/ Chemotactic factors
/ DNA damage
/ DNA topoisomerase
/ ErbB-2 protein
/ Gastric cancer
/ Gene expression
/ Histocompatibility antigen HLA
/ Humanities and Social Sciences
/ Lymphocytes T
/ Monoclonal antibodies
/ multidisciplinary
/ Science
/ Science (multidisciplinary)
/ Trastuzumab
/ Tumor cells
/ Tumors
2021
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The effects of T-DXd on the expression of HLA class I and chemokines CXCL9/10/11 in HER2-overexpressing gastric cancer cells
by
Mimura, Kosaku
, Watanabe, Yohei
, Saito, Motonobu
, Matsumoto, Takuro
, Neupane, Prajwal
, Thar Min, Aung Kyi
, Hanayama, Hiroyuki
, Ito, Misato
, Okayama, Hirokazu
, Kanke, Yasuyuki
, Nakajima, Shotaro
, Hayase, Suguru
, Saze, Zenichiro
, Nakano, Hiroshi
, Momma, Tomoyuki
, Kono, Koji
in
631/250/580
/ 631/67/1504
/ CD8 antigen
/ Cell proliferation
/ Chemokines
/ Chemotactic factors
/ DNA damage
/ DNA topoisomerase
/ ErbB-2 protein
/ Gastric cancer
/ Gene expression
/ Histocompatibility antigen HLA
/ Humanities and Social Sciences
/ Lymphocytes T
/ Monoclonal antibodies
/ multidisciplinary
/ Science
/ Science (multidisciplinary)
/ Trastuzumab
/ Tumor cells
/ Tumors
2021
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The effects of T-DXd on the expression of HLA class I and chemokines CXCL9/10/11 in HER2-overexpressing gastric cancer cells
Journal Article
The effects of T-DXd on the expression of HLA class I and chemokines CXCL9/10/11 in HER2-overexpressing gastric cancer cells
2021
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Overview
Trastuzumab deruxtecan (T-DXd), a HER2-targeting antibody–drug conjugate with a topoisomerase I inhibitor deruxtecan (DXd), exhibits an excellent anti-tumor effect in previously treated HER2-positive tumors. A recent study demonstrated that T-DXd not only suppressed tumor growth but also enhanced anti-tumor immunity through increasing the number of tumor-infiltrating CD8
+
T cells and enhancement of major-histocompatibility-complex class I expression on tumor cells in a mouse model. However, the effect of T-DXd on anti-tumor immune responses in human cancers is largely unknown. We investigated the effect of T-DXd on the expression of HLA class I and CXCL9/10/11, T-cell chemoattractants, in HER2-positive human gastric cancer (GC) cells. We found that T-DXd significantly inhibited GC cell proliferation in a HER2-dependent manner, while it slightly increased the expression of HLA class I in HER2-positive GC cells. Moreover, we revealed that T-DXd significantly induced mRNA expression of
CXCL9/10/11
in HER2-positive GC cells. T-DXd-triggered up-regulation of these chemokines was mediated through the activation of DNA damage signaling pathways. These results suggest that T-DXd triggers anti-tumor immune responses at least in part through induction of the expression of HLA class I and
CXCL9/10/11
on HER2-positive GC cells, resulting in the enhancement of anti-tumor immunity in human GC.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
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