Combinatorial drug therapy for cancer in the post-genomic era

B Al-Lazikani, U Banerji, P Workman - Nature biotechnology, 2012 - nature.com
Over the past decade, whole genome sequencing and other'omics' technologies have
defined pathogenic driver mutations to which tumor cells are addicted. Such addictions …

[HTML][HTML] Antibody-drug conjugates—an emerging class of cancer treatment

N Diamantis, U Banerji - British journal of cancer, 2016 - nature.com
Antibody-drug conjugates (ADCs) are an emerging novel class of anticancer treatment
agents that combines the selectivity of targeted treatment with the cytotoxic potency of …

Exploiting the folate receptor α in oncology

M Scaranti, E Cojocaru, S Banerjee… - Nature reviews clinical …, 2020 - nature.com
Folate receptor α (FRα) came into focus as an anticancer target many decades after the
successful development of drugs targeting intracellular folate metabolism, such as …

[PDF][PDF] Phase I pharmacokinetic and pharmacodynamic study of 17-allylamino, 17-demethoxygeldanamycin in patients with advanced malignancies

U Banerji, A O'Donnell, M Scurr, S Pacey… - Journal of Clinical …, 2005 - researchgate.net
Phase I Pharmacokinetic and Pharmacodynamic Study of 17-Allylamino, 17-Demethoxygeldanamycin
in Patients With Advanced Malignanc Page 1 Phase I Pharmacokinetic and Pharmacodynamic …

Trastuzumab duocarmazine in locally advanced and metastatic solid tumours and HER2-expressing breast cancer: a phase 1 dose-escalation and dose-expansion …

U Banerji, CML van Herpen, C Saura… - The Lancet …, 2019 - thelancet.com
Background Trastuzumab duocarmazine is a novel HER2-targeting antibody–drug
conjugate comprised of trastuzumab covalently bound to a linker drug containing …

Heat shock protein 90 as a drug target: some like it hot

U Banerji - Clinical Cancer Research, 2009 - AACR
Abstract Heat shock protein 90 (HSP90) is a ubiquitously expressed chaperone that is
involved in the posttranslational folding and stability of proteins. Inhibition at the NH2 …

Combine and conquer: challenges for targeted therapy combinations in early phase trials

JS Lopez, U Banerji - Nature reviews Clinical oncology, 2017 - nature.com
Our increasing understanding of cancer biology has led to the development of molecularly
targeted anticancer drugs. The full potential of these agents has not, however, been …

[HTML][HTML] AKT inhibition in solid tumors with AKT1 mutations

DM Hyman, LM Smyth, MTA Donoghue… - Journal of Clinical …, 2017 - ncbi.nlm.nih.gov
Purpose AKT1 E17K mutations are oncogenic and occur in many cancers at a low
prevalence. We performed a multihistology basket study of AZD5363, an ATP-competitive …

Targeting the molecular chaperone heat shock protein 90 (HSP90): lessons learned and future directions

DS Hong, U Banerji, B Tavana, GC George… - Cancer treatment …, 2013 - Elsevier
Due to the critical role of heat shock protein 90 (HSP90) in regulating the stability, activity
and intracellular sorting of its client proteins involved in multiple oncogenic processes …

[HTML][HTML] Phase I trial of first-in-class ATR inhibitor M6620 (VX-970) as monotherapy or in combination with carboplatin in patients with advanced solid tumors

TA Yap, B O'Carrigan, MS Penney, JS Lim… - Journal of Clinical …, 2020 - ncbi.nlm.nih.gov
Phase I Trial of First-in-Class ATR Inhibitor M6620 (VX-970) as Monotherapy or in Combination
With Carboplatin in Patients With Advanced Solid Tumors - PMC Back to Top Skip to main …