2020
DOI: 10.1063/1674-0068/cjcp1909168
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Theoretical investigation on QSAR of (2-Methyl-3-biphenylyl) methanol analogs as PD-L1 inhibitor

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Cited by 2 publications
(1 citation statement)
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“…Several studies have indicated that the interaction of PD-L1 with programmed cell death protein 1 (PD-1) results in tumor immune escape, consequently promoting tumor development and metastasis. Inhibiting these interactions can reactivate the toxic effect of T-cells and inhibit tumor proliferation [ [5] , [6] , [7] ]. However, clinical research showed that only a small group of patients can benefit from anti-PD-L1 inhibitors; the overall response rate is <30% [ [8] , [9] , [10] ].…”
Section: Introductionmentioning
confidence: 99%
“…Several studies have indicated that the interaction of PD-L1 with programmed cell death protein 1 (PD-1) results in tumor immune escape, consequently promoting tumor development and metastasis. Inhibiting these interactions can reactivate the toxic effect of T-cells and inhibit tumor proliferation [ [5] , [6] , [7] ]. However, clinical research showed that only a small group of patients can benefit from anti-PD-L1 inhibitors; the overall response rate is <30% [ [8] , [9] , [10] ].…”
Section: Introductionmentioning
confidence: 99%