TY - JOUR
T1 - Novel receptor tyrosine kinase targeted combination therapies for imatinib-resistant gastrointestinal stromal tumors (GIST)
AU - Mahadevan, Daruka
AU - Theiss, Noah
AU - Morales, Carla
AU - Stejskal, Amy E.
AU - Cooke, Laurence S.
AU - Zhu, Min
AU - Kurtzman, Drew
AU - Swart, Rachel
AU - Ong, Evan
AU - Qi, Wenqing
PY - 2015
Y1 - 2015
N2 - Background: c-Kit/α-PDGFR targeted therapies are effective for gastrointestinal stromal tumors (GIST), but, >50% develop drug resistance. Methods: RTK expression (c-Kit, c-Met, AXL, HER-1, HER-2, IGF-1R) in pre-/post-imatinib (IM) GIST patient samples (n=16) and 4 GIST cell lines were examined for RTK inhibitor activity. GIST-882 cells were cultured in IM every other day, cells collected (1 week to 6 months) and analyzed by qRT-PCR and Western blotting. Results: Immunohistochemistry pre-/post-IM demonstrated continued expression of c-Kit and HER1, while a subset expressed IGF-1R, c-Met and AXL. In GIST cells (GIST-882, GIST430/654, GIST48) c-Kit, HER1 and c-Met are co-expressed. Acute IM over-express c-Kit while chronic IM, lose c-Kit and HER-1 in GIST882 cells. GIST882 and GIST430/654 cells have an IC50 0.077 and 0.59 μM to IM respectively. GIST48 have an IC50 0.66 μM to IM, 0.91 μM to amuvatinib [AMU] and 0.67 μM to erlotinib (Erl). Synergistic combinations: GIST882, AMU + Erl (CI 0.20); IM + AMU (CI 0.50), GIST430/654, IM + afatinib (CI 0.39); IM + AMU (CI 0.42), GIST48, IM + afatinib (CI 0.03); IM + AMU (CI 0.04); AMU + afatinib (CI 0.36); IM + Erl (CI 0.63). Conclusion: Targeting c-Kit plus HER1 or AXL/c-Met abrogates IM resistance in GIST.
AB - Background: c-Kit/α-PDGFR targeted therapies are effective for gastrointestinal stromal tumors (GIST), but, >50% develop drug resistance. Methods: RTK expression (c-Kit, c-Met, AXL, HER-1, HER-2, IGF-1R) in pre-/post-imatinib (IM) GIST patient samples (n=16) and 4 GIST cell lines were examined for RTK inhibitor activity. GIST-882 cells were cultured in IM every other day, cells collected (1 week to 6 months) and analyzed by qRT-PCR and Western blotting. Results: Immunohistochemistry pre-/post-IM demonstrated continued expression of c-Kit and HER1, while a subset expressed IGF-1R, c-Met and AXL. In GIST cells (GIST-882, GIST430/654, GIST48) c-Kit, HER1 and c-Met are co-expressed. Acute IM over-express c-Kit while chronic IM, lose c-Kit and HER-1 in GIST882 cells. GIST882 and GIST430/654 cells have an IC50 0.077 and 0.59 μM to IM respectively. GIST48 have an IC50 0.66 μM to IM, 0.91 μM to amuvatinib [AMU] and 0.67 μM to erlotinib (Erl). Synergistic combinations: GIST882, AMU + Erl (CI 0.20); IM + AMU (CI 0.50), GIST430/654, IM + afatinib (CI 0.39); IM + AMU (CI 0.42), GIST48, IM + afatinib (CI 0.03); IM + AMU (CI 0.04); AMU + afatinib (CI 0.36); IM + Erl (CI 0.63). Conclusion: Targeting c-Kit plus HER1 or AXL/c-Met abrogates IM resistance in GIST.
KW - Amuvatinib
KW - Erlotinib
KW - Gist
KW - HER-1
KW - Imatinib
KW - c-Kit
UR - http://www.scopus.com/inward/record.url?scp=84923033184&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84923033184&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.3021
DO - 10.18632/oncotarget.3021
M3 - Article
C2 - 25557174
AN - SCOPUS:84923033184
SN - 1949-2553
VL - 6
SP - 1954
EP - 1966
JO - Oncotarget
JF - Oncotarget
IS - 4
ER -