TY  - JOUR
N1  - Copyright of this article belongs to NPG.
ID  - open1703
UR  - http://www.nature.com/srep/2014/140327/srep04483/full/srep04483.html
A1  - Ahmad, Sahil
A1  - Gupta, Sudheer
A1  - Kumar, Rahul
A1  - Varshney, Grish C
A1  - Raghava, G.P.S.
Y1  - 2014///
N2  - Monoclonal antibody Trastuzumab/Herceptin is considered as frontline therapy for Her2-positive breast cancer patients. However, it is not effective against several patients due to acquired or de novo resistance. In last one decade, several assays have been performed to understand the mechanism of Herceptin resistance with/without supplementary drugs. This manuscript describes a database HerceptinR, developed for understanding the mechanism of resistance at genetic level. HerceptinR maintains information about 2500 assays performed against various breast cancer cell lines (BCCs), for improving sensitivity of Herceptin with or without supplementary drugs. In order to understand Herceptin resistance at genetic level, we integrated genomic data of BCCs that include expression, mutations and copy number variations in different cell lines. HerceptinR will play a vital role in i) designing biomarkers to identify patients eligible for Herceptin treatment and ii) identification of appropriate supplementary drug for a particular patient. HerceptinR is available at http://crdd.osdd.net/raghava/herceptinr/.
PB  - Nature Publishing Group
JF  - Scientific reports
VL  - 4
KW  - Database; Breast Cancer
SN  - 2045-2322
TI  - Herceptin resistance database for understanding mechanism of resistance in breast cancer patients.
ER  -