scispace - formally typeset
Open AccessJournal ArticleDOI

Harnessing synthetic lethal interactions in anticancer drug discovery

Reads0
Chats0
TLDR
Strategies that can be used to identify synthetic lethal interactions for anticancer drug discovery are summarized, examples of such interactions that are currently being investigated in preclinical and clinical studies of targeted anticancer therapies are described, and the challenges of realizing the full potential of such therapies are discussed.
Abstract
Unique features of tumours that can be exploited by targeted therapies are a key focus of current cancer research. One such approach is known as synthetic lethality screening, which involves searching for genetic interactions of two mutations whereby the presence of either mutation alone has no effect on cell viability but the combination of the two mutations results in cell death. The presence of one of these mutations in cancer cells but not in normal cells can therefore create opportunities to selectively kill cancer cells by mimicking the effect of the second genetic mutation with targeted therapy. Here, we summarize strategies that can be used to identify synthetic lethal interactions for anticancer drug discovery, describe examples of such interactions that are currently being investigated in preclinical and clinical studies of targeted anticancer therapies, and discuss the challenges of realizing the full potential of such therapies.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

The NAD metabolome — a key determinant of cancer cell biology

TL;DR: Given that NAD+-dependent signalling reactions involve the degradation of the molecule, permanent nucleotide resynthesis through different biosynthetic pathways is crucial for incessant cancer cell proliferation, this necessity supports the targeting of NAD metabolism as a new therapeutic concept for cancer treatment.
Journal ArticleDOI

Phenotypic screening in cancer drug discovery — past, present and future

TL;DR: It is postulate that the contribution of phenotypic screening to cancer drug discovery has been hampered by a reliance on 'classical' nonspecific drug effects such as cytotoxicity and mitotic arrest, exacerbated by a paucity of mechanistically defined cellular models for therapeutically translatable cancer phenotypes.
Journal ArticleDOI

Target Identification for Small Bioactive Molecules: Finding the Needle in the Haystack

TL;DR: Current methods for target identification of small molecules are summarized, primarily for a chemistry audience but also the biological community, for example, the chemist or biologist attempting to identify the target of a given bioactive compound.
Journal ArticleDOI

Deubiquitinases in cancer: new functions and therapeutic options

TL;DR: Understanding of the physiological regulatory mechanisms of these enzymes may provide answers to multiple remaining questions on DUB functions and lead to the development of DUB-targeting strategies to expand the repertoire of molecular therapies against cancer.
References
More filters
Journal ArticleDOI

Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy

TL;DR: BRCA1 or BRCA2 dysfunction unexpectedly and profoundly sensitizes cells to the inhibition of PARP enzymatic activity, resulting in chromosomal instability, cell cycle arrest and subsequent apoptosis, illustrating how different pathways cooperate to repair damage.
Journal ArticleDOI

Sunitinib versus interferon alfa in metastatic renal-cell carcinoma.

TL;DR: Progression-free survival was longer and response rates were higher in patients with metastatic renal-cell cancer who received sunitinib than in those receiving interferon alfa.
Related Papers (5)