TY - JOUR
T1 - Targeting the RNA polymerase i transcription for cancer therapy comes of age
AU - Ferreira, Rita
AU - Schneekloth, John S.
AU - Panov, Konstantin I.
AU - Hannan, Katherine M.
AU - Hannan, Ross D.
N1 - Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/2
Y1 - 2020/2
N2 - Transcription of the ribosomal RNA genes (rDNA) that encode the three largest ribosomal RNAs (rRNA), is mediated by RNA Polymerase I (Pol I) and is a key regulatory step for ribosomal biogenesis. Although it has been reported over a century ago that the number and size of nucleoli, the site of ribosome biogenesis, are increased in cancer cells, the significance of this observation for cancer etiology was not understood. The realization that the increase in rRNA expression has an active role in cancer progression, not only through increased protein synthesis and thus proliferative capacity but also through control of cellular check points and chromatin structure, has opened up new therapeutic avenues for the treatment of cancer through direct targeting of Pol I transcription. In this review, we discuss the rational of targeting Pol I transcription for the treatment of cancer; review the current cancer therapeutics that target Pol I transcription and discuss the development of novel Pol I‐specific inhibitors, their therapeutic potential, challenges and future prospects.
AB - Transcription of the ribosomal RNA genes (rDNA) that encode the three largest ribosomal RNAs (rRNA), is mediated by RNA Polymerase I (Pol I) and is a key regulatory step for ribosomal biogenesis. Although it has been reported over a century ago that the number and size of nucleoli, the site of ribosome biogenesis, are increased in cancer cells, the significance of this observation for cancer etiology was not understood. The realization that the increase in rRNA expression has an active role in cancer progression, not only through increased protein synthesis and thus proliferative capacity but also through control of cellular check points and chromatin structure, has opened up new therapeutic avenues for the treatment of cancer through direct targeting of Pol I transcription. In this review, we discuss the rational of targeting Pol I transcription for the treatment of cancer; review the current cancer therapeutics that target Pol I transcription and discuss the development of novel Pol I‐specific inhibitors, their therapeutic potential, challenges and future prospects.
KW - CX‐5461
KW - Cancer therapy
KW - RNA polymerase I transcription
KW - Ribosome biogenesis
UR - http://www.scopus.com/inward/record.url?scp=85080863573&partnerID=8YFLogxK
U2 - 10.3390/cells9020266
DO - 10.3390/cells9020266
M3 - Review article
SN - 2073-4409
VL - 9
JO - Cells
JF - Cells
IS - 2
M1 - 266
ER -