2023
DOI: 10.1016/j.jsps.2022.11.007
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Construction and stable gene expression of AGR2xPD1 bi-specific antibody that enhances attachment between T-Cells and lung tumor cells, suppress tumor cell migration and promoting CD8 expression in cytotoxic T-cells

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Cited by 4 publications
(3 citation statements)
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“…For instance, Roy et al demonstrated an augmented tumorkilling effect by developing BsAb-AGR2×PD1 for AGR2-positive cancers, intercepting AGR2 paracrine signaling, and rerouting cytotoxic T-cells towards AGR2+ cancer cells to reduce tumor cell viability [135]. These enhanced tumor-killing effects, primarily exploiting AGR2 overexpression in tumor cells, could enhance the efficacy of monoclonal antibody therapy [135]. We posit that AGR2 has already paved the way for novel discoveries regarding its therapeutic role in cancer.…”
Section: Agr2 and Clinical Treatmentmentioning
confidence: 92%
See 1 more Smart Citation
“…For instance, Roy et al demonstrated an augmented tumorkilling effect by developing BsAb-AGR2×PD1 for AGR2-positive cancers, intercepting AGR2 paracrine signaling, and rerouting cytotoxic T-cells towards AGR2+ cancer cells to reduce tumor cell viability [135]. These enhanced tumor-killing effects, primarily exploiting AGR2 overexpression in tumor cells, could enhance the efficacy of monoclonal antibody therapy [135]. We posit that AGR2 has already paved the way for novel discoveries regarding its therapeutic role in cancer.…”
Section: Agr2 and Clinical Treatmentmentioning
confidence: 92%
“…Moreover, AGR2 can be leveraged as a monoclonal antibody, such as 18A4, to enhance the efficacy of other cancer treatments, significantly augmenting the inhibitory impact of drugs on cancer cells [74]. For instance, Roy et al demonstrated an augmented tumorkilling effect by developing BsAb-AGR2×PD1 for AGR2-positive cancers, intercepting AGR2 paracrine signaling, and rerouting cytotoxic T-cells towards AGR2+ cancer cells to reduce tumor cell viability [135]. These enhanced tumor-killing effects, primarily exploiting AGR2 overexpression in tumor cells, could enhance the efficacy of monoclonal antibody therapy [135].…”
Section: Agr2 and Clinical Treatmentmentioning
confidence: 99%
“…Roy et al. ( 106 ) designed and synthesized BsAb AGR2xPD1, which showed higher anti-tumor response compared with the group of 18A4HU monoclonal antibody (mAb), the group of PD1 mAb and the combination treatment group of 18A4HU mAb and PD1 mAb. Wang et al.…”
Section: Potential Therapeutic Targets In Breast Cancermentioning
confidence: 99%