VCR chemotherapy, HDAC inhibition, and SMARCA4 inhibition

NB Narendra Bharathy
NB Noah E. Berlow
EW Eric Wang
JA Jinu Abraham
TS Teagan P. Settelmeyer
JH Jody E. Hooper
MS Matthew N. Svalina
YI Yoshihiro Ishikawa
KZ Keith Zientek
ZB Zia Bajwa
MG Martin W. Goros
BH Brian S. Hernandez
JW Johannes E. Wolff
MR Michelle A. Rudek
LX Linping Xu
NA Nicole M. Anders
RP Ranadip Pal
AH Alexandria P. Harrold
AD Angela M. Davies
AA Arya Ashok
DB Darnell Bushby
MM Maria Mancini
CN Christopher Noakes
NG Neal C. Goodwin
PO Peter Ordentlich
JK James Keck
DH Douglas S. Hawkins
ER Erin R. Rudzinski
BC Bishwanath Chatterjee
HB Hans Peter Bächinger
FB Frederic G. Barr
JL Jennifer Liddle
BG Benjamin A. Garcia
AM Atiya Mansoor
TP Theodore J. Perkins
CV Christopher R. Vakoc
JM Joel E. Michalek
CK Charles Keller
ask Ask a question
Favorite

The chemotherapy agent VCR sulfate, used here in the treatment of Rh30 and U23674 cells, was obtained from Sigma (product no. V8879). HDACis used in this study were purchased from Selleckchem: ENT (also known as MS-275, a class I HDACi; catalog no. S1053), PAN (a broad-spectrum HDACi; catalog no. S1030), SAHA (catalog no. S1047), CUDC-907 (a PI3K inhibitor and a class I and class II HDACi; catalog no. S2759), and CUDC-101 (a class I and class II HDACi and an inhibitor of epidermal growth factor receptor family members EGFR and HER2; catalog no. S1194). aRMS cell lines and primary tumor cell cultures were treated with these drugs at their clinically relevant Cmax (maximum plasma concentrations) or, where Cmax is not yet reported, their determined IC25.

Do you have any questions about this protocol?

Post your question to gather feedback from the community. We will also invite the authors of this article to respond.

post Post a Question
0 Q&A