Logo-apb
Submitted: 07 Oct 2024
Revision: 02 Jun 2025
Accepted: 04 Jun 2025
ePublished: 11 Jun 2025
EndNote EndNote

(Enw Format - Win & Mac)

BibTeX BibTeX

(Bib Format - Win & Mac)

Bookends Bookends

(Ris Format - Mac only)

EasyBib EasyBib

(Ris Format - Win & Mac)

Medlars Medlars

(Txt Format - Win & Mac)

Mendeley Web Mendeley Web
Mendeley Mendeley

(Ris Format - Win & Mac)

Papers Papers

(Ris Format - Win & Mac)

ProCite ProCite

(Ris Format - Win & Mac)

Reference Manager Reference Manager

(Ris Format - Win only)

Refworks Refworks

(Refworks Format - Win & Mac)

Zotero Zotero

(Ris Format - Firefox Plugin)

Adv Pharm Bull. Inpress.
doi: 10.34172/apb.025.43819
  Abstract View: 24

Research Article

MicroRNA-Mediated Silencing of Calumenin: A Potential Strategy for Inhibiting Proliferation and Migration in Breast Cancer Cells

Zahra Amiri ORCID logo, Fatemeh Bahrami, Babak Jahangiri ORCID logo, Arash Javeri, Frouzandeh Mahjoubi, Nahid Nafissi, Mohammad Zaefizadeh, Fatemeh Masoumi, Alireza Zomorodipour* ORCID logo
*Corresponding Author: Email: zomorodi@nigeb.ac.ir

Abstract

Background: Calumenin is a calcium-binding protein involved in several physiological processes, exhibiting tumor-specific expression variation and emerging as a potential player in cancer progression.

Purpose: This study aimed to investigate the correlation between CALU and clinicopathological features in breast cancer (BC) and perform a functional assessment of CALU based on a microRNA-mediated knockdown approach.

Methods: The BC tissues' CALU expression was measured by q-RT-PCR. We looked at correlations between changes in CALU expression and clinicopathological characteristics. We adopted a CALU knockdown approach using an artificial microRNA, expressed through an episomal vector, in BC cell lines. Epithelial to mesenchymal transition (EMT) markers were then assessed, and cell cycle, migration, proliferation, and apoptosis were analyzed.

Results: When compared to the normal surrounding tissues, the BC tissues showed a 3.4-fold increase in CALU expression. This was significantly correlated with clinicopathological parameters such as histological grade, Ki-67 expression, TNM stage, lymph node involvement, and vascular lymph invasion. Key EMT markers, including GSC, MMP2, TIMP1, TGF1, SLUG, ZEB1, ZEB2, SNALI1, and TWIST1, were downregulated as a result of CALU knockdown, which prevented cell migration and proliferation and caused cell cycle arrest and apoptosis in the BC cell lines.

Conclusion: The results of the miRNA-mediated knockdown approach support the findings that CALU is a potential promoter of breast cancer (BC), as evidenced by the upregulation of CALU in BC tissues and its correlation with clinicopathological features, which highlights its role in breast cancer progression.


First Name
Last Name
Email Address
Comments
Security code


Abstract View: 21

Your browser does not support the canvas element.


PDF Download: 0

Your browser does not support the canvas element.