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Drugging the undruggable: Transcription therapy for cancer

*Corresponding author for this work
  • Albany Medical College
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Transcriptional regulation is often the convergence point of oncogenic signaling. It is not surprising, therefore, that aberrant gene expression is a hallmark of cancer. Transformed cells often develop a dependency on such a reprogramming highlighting the therapeutic potential of rectifying cancer-associated transcriptional abnormalities in malignant cells. Although transcription is traditionally considered as undruggable, agents have been developed that target various levels of transcriptional regulation including DNA binding by transcription factors, protein-protein interactions, and epigenetic alterations. Some of these agents have been approved for clinical use or entered clinical trials. While artificial transcription factors have been developed that can theoretically modulate expression of any given gene, the emergence of reliable reporter assays greatly facilitates the search for transcription-targeted agents. This review provides a comprehensive overview of these developments, and discusses various strategies applicable for developing transcription-targeted therapeutic agents.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 76-85 (10 pages)

Journal (Volume, Issue Number)

Biochimica et Biophysica Acta - Reviews on Cancer (Volume 1835, Issue 1)

Publication milestones

  • Published - 01/2013

Publication status

Published - 01/2013

ISSN

0304-419X

Publication IDs

  • Scopus: 84869861385
  • PubMed: 23147197

Publication metrics

Metrics

SciVal
FWCI
1.68
SciVal
Author count
2
SciVal
citations
77
SciVal
Paper percentile
96
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1
Scopus
citations

PlumX, opens in new tab

Captures
177
Mentions
1
Citation count
104

Funding Details

This work was supported by NIH grants R01CA164006 and R01CA139107 to CY and R01GM057242 to PJH.
FundersFunding numbers
NIH
R01GM057242, R01CA164006
NCI
R01CA139107