[HTML][HTML] Triple-negative breast cancer molecular subtyping and treatment progress

L Yin, JJ Duan, XW Bian, S Yu - Breast Cancer Research, 2020 - Springer
Triple-negative breast cancer (TNBC), a specific subtype of breast cancer that does not
express estrogen receptor (ER), progesterone receptor (PR), or human epidermal growth …

[HTML][HTML] Triple-negative breast cancer: current understanding and future therapeutic breakthrough targeting cancer stemness

KL Lee, YC Kuo, YS Ho, YH Huang - Cancers, 2019 - mdpi.com
Triple-negative breast cancer (TNBC) is cancer that tested as negative for estrogen
receptors (ER), progesterone receptors (PR), and excess human epidermal growth factor …

Randomized, double-blind, phase II study of temozolomide in combination with either veliparib or placebo in patients with relapsed-sensitive or refractory small-cell …

MC Pietanza, SN Waqar, LM Krug, A Dowlati… - Journal of Clinical …, 2018 - ascopubs.org
Purpose Both temozolomide (TMZ) and poly (ADP-ribose) polymerase (PARP) inhibitors are
active in small-cell lung cancer (SCLC). This phase II, randomized, double-blind study …

Biology, metastatic patterns, and treatment of patients with triple-negative breast cancer

CK Anders, LA Carey - Clinical breast cancer, 2009 - Elsevier
Of the estimated 1 million cases of breast cancer diagnosed annually worldwide, it is
estimated that over 170,000 will harbor the triple-negative (estrogen receptor/progesterone …

Using sulfuramidimidoyl fluorides that undergo sulfur(vi) fluoride exchange for inverse drug discovery

GJ Brighty, RC Botham, S Li, L Nelson… - Nature …, 2020 - nature.com
Drug candidates that form covalent linkages with their target proteins have been
underexplored compared with the conventional counterparts that modulate biological …

A review of systemic treatment in metastatic triple-negative breast cancer

SB Zeichner, H Terawaki… - Breast cancer: basic and …, 2016 - journals.sagepub.com
Patients with breast cancer along with metastatic estrogen and progesterone receptor
(ER/PR)-and human epidermal growth factor receptor 2 (HER2)-negative tumors are …

The DNA damaging revolution: PARP inhibitors and beyond.

TA Yap, R Plummer, NS Azad… - American Society of …, 2019 - europepmc.org
Cancer-specific DNA repair defects are abundant in malignant tissue and present an
opportunity to capitalize on these aberrations for therapeutic benefit. Early preclinical data …

ABT-888, an orally active poly (ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models

CK Donawho, Y Luo, Y Luo, TD Penning, JL Bauch… - Clinical cancer …, 2007 - AACR
Purpose: To evaluate the preclinical pharmacokinetics and antitumor efficacy of a novel
orally bioavailable poly (ADP-ribose) polymerase (PARP) inhibitor, ABT-888. Experimental …

4-[3-(4-Cyclopropanecarbonylpiperazine-1-carbonyl)-4-fluorobenzyl]-2H-phthalazin-1-one: A Novel Bioavailable Inhibitor of Poly(ADP-ribose) Polymerase-1

KA Menear, C Adcock, R Boulter… - Journal of medicinal …, 2008 - ACS Publications
Poly (ADP-ribose) polymerase activation is an immediate cellular response to metabolic-,
chemical-, or ionizing radiation-induced DNA damage and represents a new target for …

[HTML][HTML] The role of PARP in DNA repair and its therapeutic exploitation

M Javle, NJ Curtin - British journal of cancer, 2011 - nature.com
Historically, PARP inhibitors (PARPi) were developed to potentiate the cytotoxic effect of
certain chemotherapeutic agents and are currently being investigated in combination with …