Title : Selective Tumor Cell Apoptosis and Tumor Regression in CDH17-Positive Colorectal Cancer Models using BI 905711, a Novel Liver-Sparing TRAILR2 Agonist.

Pub. Date : 2021 Jan

PMID : 33037135






7 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Selective tumor cell apoptosis and tumor regression in CDH17-positive colorectal cancer models using BI 905711, a novel liver-sparing TRAILR2 agonist. bi 905711 cadherin 17 Homo sapiens
2 BI 905711 is a novel tetravalent bispecific antibody targeting both TRAILR2 and CDH17 and represents a novel liver-sparing TRAILR2 agonist specifically designed to overcome the disadvantages of previous strategies. bi 905711 cadherin 17 Homo sapiens
3 Here, we show that BI 905711 effectively triggered apoptosis in a broad panel of CDH17-positive CRC tumor cells in vitro. bi 905711 cadherin 17 Homo sapiens
4 BI 905711 demonstrated single-agent tumor regressions in CDH17-positive CRC xenografts, an effect that was further enhanced upon combination with irinotecan. bi 905711 cadherin 17 Homo sapiens
5 BI 905711 induced apoptosis in both a cis (same cell) as well as trans (adjacent cell) fashion, translating into significant anti-tumor activity even in xenograft models with heterogeneous CDH17 expression. bi 905711 cadherin 17 Homo sapiens
6 In summary, we demonstrate that BI 905711 has potent and selective antitumor activity in CDH17-positive colorectal cancer models both in vitro and in vivo. bi 905711 cadherin 17 Homo sapiens
7 The high prevalence of over 95 percent CDH17-positive tumors in CRC patients, the molecule preclinical efficacy together with its potential for a favorable safety profile, support the ongoing BI 905711 phase I trial in CRC and additional CDH17-positive cancer types (NCT04137289). bi 905711 cadherin 17 Homo sapiens