» Articles » PMID: 33227712

Inhibiting RRM2 to Enhance the Anticancer Activity of Chemotherapy

Overview
Date 2020 Nov 23
PMID 33227712
Citations 50
Authors
Affiliations
Soon will be listed here.
Abstract

RRM2, the small subunit of ribonucleotide reductase, is identified as a tumor promotor and therapeutic target. It is common to see the overexpression of RRM2 in chemo-resistant cancer cells and patients. RRM2 mediates the resistance of many chemotherapeutic drugs and could become the predictor for chemosensitivity and prognosis. Therefore, inhibition of RRM2 may be an effective means to enhance the anticancer activity of chemotherapy. This review tries to discuss the mechanisms of RRM2 overexpression and the role of RRM2 in resistance to chemotherapy. Additionally, we compile the studies on small interfering RNA targets RRM2, RRM2 inhibitors, kinase inhibitors, and other ways that could overcome the resistance of chemotherapy or exert synergistic anticancer activity with chemotherapy through the expression inhibition or the enzyme inactivation of RRM2.

Citing Articles

Combined inhibition of ribonucleotide reductase and WEE1 induces synergistic anticancer activity in Ewing's sarcoma cells.

Ziener J, Henao-Restrepo J, Leonhardi J, Sturm M, Becker S, Morales-Prieto D BMC Cancer. 2025; 25(1):277.

PMID: 39962391 PMC: 11831844. DOI: 10.1186/s12885-025-13691-2.


Fast-Relaxing Hydrogels Promote Pancreatic Adenocarcinoma Cell Aggressiveness through Integrin β1 Signaling.

Nguyen H, Luong N, Peil J, Tong Y, Mitchell D, Fishel M Biomacromolecules. 2025; 26(2):1098-1110.

PMID: 39841789 PMC: 11817685. DOI: 10.1021/acs.biomac.4c01441.


Silencing circ_0043256 inhibited CoCl2-induced proliferation, migration, and aerobic glycolysis in gastric cancer cells.

Ou W, Tan R, Zhai J, Sun L, Quan Z, Huang X Sci Rep. 2025; 15(1):171.

PMID: 39748101 PMC: 11697268. DOI: 10.1038/s41598-024-84548-0.


IKBKE regulates renal cell carcinoma progression and sunitinib resistance through the RRM2-AKT pathway.

Liu S, Li J, Zhang J, Wan F, Hong Z, Hong Z Int J Biol Sci. 2024; 20(15):6146-6161.

PMID: 39664571 PMC: 11628342. DOI: 10.7150/ijbs.102666.


Indirect targeting of MYC and direct targeting in combination with chemotherapies are more effective than direct mono-targeting in triple negative breast cancer.

Mekonnen N, Yang H, Rajasekaran N, Song K, Choi Y, Shin Y Transl Oncol. 2024; 51:102204.

PMID: 39631207 PMC: 11652953. DOI: 10.1016/j.tranon.2024.102204.