Calcitonin targets extracellular signal-regulated kinase signaling pathway in human cancers

20Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

Abstract

The mitogen-activated protein kinases (MAPKs) signaling pathway is a potential target in cancer therapy. Constitutive phosphorylated extracellular signal-regulated kinase (ERK1/2), which is one of the MAPKs has been detected in a variety of tumors. Calcitonin (CT) is a polypeptide hormone secreted by the thyroid gland and has been used to treat the osteoporosis and humoral hypercalcemia of malignancy. We report that CT decreases ERK1/2 phosphorylation in cancer cells showing constitutive phosphorylated ERK1/2. In MDA-MB-231 cells, a breast cancer cell line showing constitutive phosphorylated ERK1/2, CT phosphorylated c-Raf at Ser259 via the protein kinase A pathway, resulting in suppression of ERK1/2 phosphorylation. CT significantly reduced the tumor volume of MDA-MB-231 cells showing constitutive phosphorylated ERK1/2 compared with saline buffer. However, CT did not exert any significant effects on the proliferation of MCF-7 cells, a breast cancer cell line, showing non-constitutive phosphorylated ERK1/2. These novel findings indicate that CT may be used to target ERK in the treatment of cancer. © 2007 Society for Endocrinology.

Cite

CITATION STYLE

APA

Nakamura, M., Han, B., Nishishita, T., Bai, Y., & Kakudo, K. (2007). Calcitonin targets extracellular signal-regulated kinase signaling pathway in human cancers. Journal of Molecular Endocrinology, 39(5–6), 375–384. https://doi.org/10.1677/JME-07-0036

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free