» Articles » PMID: 24422040

Mechanisms of Action of Bisphosphonates in Oncology: a Scientific Concept Evolving from Antiresorptive to Anticancer Activities

Overview
Journal Bonekey Rep
Date 2014 Jan 15
PMID 24422040
Citations 34
Authors
Affiliations
Soon will be listed here.
Abstract

Bisphosphonates are approved for treating malignant bone disease from advanced cancer because they are effective inhibitors of osteoclast-mediated bone resorption. However, there may be a greater role for the use of bisphosphonates than has previously been considered. There is a large body of preclinical evidence showing that bisphosphonates exert a variety of direct and indirect anticancer activities that affect both tumor cells and the surrounding microenvironment, and that stimulate immune reactions. Recent data from clinical trials have shown that adding the bisphosphonate zoledronate to endocrine therapy or chemotherapy improves disease-free survival of patients with endocrine-responsive early breast cancer in a low estrogen environment (that is, following ovarian suppression therapy or in women with established menopause at diagnosis). Adjuvant treatment with the bisphosphonate clodronate also improves disease-free survival in postmenopausal breast cancer. Additionally, zoledronate was found to prolong survival in patients with symptomatic multiple myeloma or other advanced cancers. Here, we present an overview of preclinical and clinical studies that demonstrate anticancer benefits of bisphosphonates, and we discuss potential mechanisms of action that might be responsible for the anticancer activity of bisphosphonates in the clinic.

Citing Articles

Determinants of outcome in cancer patients with medication-related osteonecrosis of the jaw: A 19-year retrospective study.

Ward J, Singh A, White C, Riedel E, Lewis R, Yom S Oral Oncol Rep. 2024; 10.

PMID: 38957376 PMC: 11218890. DOI: 10.1016/j.oor.2024.100488.


Effects of neoadjuvant zoledronate and radiation therapy on cell survival, cell cycle distribution, and clinical status in canine osteosarcoma.

Norquest C, Rogic A, Gimotty P, Maitz C, Rindt H, Ashworth H Front Vet Sci. 2024; 11:1237084.

PMID: 38362299 PMC: 10867971. DOI: 10.3389/fvets.2024.1237084.


Role of mitochondrial alterations in human cancer progression and cancer immunity.

Wang S, Tseng L, Lee H J Biomed Sci. 2023; 30(1):61.

PMID: 37525297 PMC: 10392014. DOI: 10.1186/s12929-023-00956-w.


Osteoclast-mediated resorption primes the skeleton for successful integration during axolotl limb regeneration.

Riquelme-Guzman C, Tsai S, Carreon Paz K, Nguyen C, Oriola D, Schuez M Elife. 2022; 11.

PMID: 36218256 PMC: 9581535. DOI: 10.7554/eLife.79966.


Effects of Bisphosphonate on Osteocyte Proliferation and Bone Formation in Patients with Diabetic Osteoporosis.

Weng B, Chen C Comput Math Methods Med. 2022; 2022:2368564.

PMID: 35844452 PMC: 9279083. DOI: 10.1155/2022/2368564.


References
1.
Benzaid I, Monkkonen H, Bonnelye E, Monkkonen J, Clezardin P . In vivo phosphoantigen levels in bisphosphonate-treated human breast tumors trigger Vγ9Vδ2 T-cell antitumor cytotoxicity through ICAM-1 engagement. Clin Cancer Res. 2012; 18(22):6249-59. DOI: 10.1158/1078-0432.CCR-12-0918. View

2.
Coscia M, Quaglino E, Iezzi M, Curcio C, Pantaleoni F, Riganti C . Zoledronic acid repolarizes tumour-associated macrophages and inhibits mammary carcinogenesis by targeting the mevalonate pathway. J Cell Mol Med. 2009; 14(12):2803-15. PMC: 3822730. DOI: 10.1111/j.1582-4934.2009.00926.x. View

3.
Kunzmann V, Bauer E, Feurle J, Weissinger F, Tony H, Wilhelm M . Stimulation of gammadelta T cells by aminobisphosphonates and induction of antiplasma cell activity in multiple myeloma. Blood. 2000; 96(2):384-92. View

4.
Kim M, Oskarsson T, Acharyya S, Nguyen D, Zhang X, Norton L . Tumor self-seeding by circulating cancer cells. Cell. 2010; 139(7):1315-26. PMC: 2810531. DOI: 10.1016/j.cell.2009.11.025. View

5.
Khalili H, Huang E, Ogino S, Fuchs C, Chan A . A prospective study of bisphosphonate use and risk of colorectal cancer. J Clin Oncol. 2012; 30(26):3229-33. PMC: 3434982. DOI: 10.1200/JCO.2011.39.2670. View