» Articles » PMID: 24611128

Epithelial-mesenchymal Transition---A Hallmark of Breast Cancer Metastasis

Overview
Journal Cancer Hallm
Date 2014 Mar 11
PMID 24611128
Citations 86
Authors
Affiliations
Soon will be listed here.
Abstract

Epithelial-mesenchymal transition (EMT) is a highly conserved cellular program that converts polarized, immotile epithelial cells to migratory mesenchymal cells. In addition, EMT was initially recognized as a key step for morphogenesis during embryonic development. Emerging evidences indicate that this important developmental program promotes metastasis, drug resistance, and tumor recurrence, features that are associated with a poor clinical outcome for patients with breast cancer. Therefore, better understanding of regulation and signaling pathways in EMT is essential to develop novel targeted therapeutics. In this review, we present updated developments underlying EMT in tumor progression and metastasis, and discuss the challenges remaining in breast cancer research.

Citing Articles

Reactive oxygen species induced by SARS-CoV-2 infection can induce EMT in solid tumors: Potential role of COVID-19 in chemo-resistance and metastasis.

Moulaeian M, Ferdousmakan S, Banihashemi S, Homayounfar S, Pasupulla A, Malekzadegan Y Heliyon. 2024; 10(22):e40297.

PMID: 39624316 PMC: 11609686. DOI: 10.1016/j.heliyon.2024.e40297.


UGT1A7 altered HER2-positive breast cancer response to trastuzumab by affecting epithelial-to-mesenchymal transition: A potential biomarker to identify patients resistant to trastuzumab treatment.

Wang C, Bai C, Zhang Z, Zhou H, Gao H, Wang S Cancer Gene Ther. 2024; 31(10):1525-1535.

PMID: 39122832 DOI: 10.1038/s41417-024-00819-y.


Reconstruction of single-cell lineage trajectories and identification of diversity in fates during the epithelial-to-mesenchymal transition.

Cheng Y, Zhang Y, Tripathi S, Harshavardhan B, Jolly M, Schiebinger G Proc Natl Acad Sci U S A. 2024; 121(32):e2406842121.

PMID: 39093947 PMC: 11317558. DOI: 10.1073/pnas.2406842121.


Identifying Key Genes Involved in Axillary Lymph Node Metastasis in Breast Cancer Using Advanced RNA-Seq Analysis: A Methodological Approach with GLMQL and MAS.

Rezapour M, Wesolowski R, Gurcan M Int J Mol Sci. 2024; 25(13).

PMID: 39000413 PMC: 11242629. DOI: 10.3390/ijms25137306.


Exosome-sheathed porous silica nanoparticle-mediated co-delivery of 3,3'-diindolylmethane and doxorubicin attenuates cancer stem cell-driven EMT in triple negative breast cancer.

Sarkar R, Biswas S, Ghosh R, Samanta P, Pakhira S, Mondal M J Nanobiotechnology. 2024; 22(1):285.

PMID: 38796426 PMC: 11127288. DOI: 10.1186/s12951-024-02518-0.


References
1.
Zhang Z, Huang L, Zhao W, Rigas B . Annexin 1 induced by anti-inflammatory drugs binds to NF-kappaB and inhibits its activation: anticancer effects in vitro and in vivo. Cancer Res. 2010; 70(6):2379-88. PMC: 2953961. DOI: 10.1158/0008-5472.CAN-09-4204. View

2.
Brabletz S, Brabletz T . The ZEB/miR-200 feedback loop--a motor of cellular plasticity in development and cancer?. EMBO Rep. 2010; 11(9):670-7. PMC: 2933868. DOI: 10.1038/embor.2010.117. View

3.
Wang Z, Banerjee S, Li Y, Rahman K, Zhang Y, Sarkar F . Down-regulation of notch-1 inhibits invasion by inactivation of nuclear factor-kappaB, vascular endothelial growth factor, and matrix metalloproteinase-9 in pancreatic cancer cells. Cancer Res. 2006; 66(5):2778-84. DOI: 10.1158/0008-5472.CAN-05-4281. View

4.
Loges S, Mazzone M, Hohensinner P, Carmeliet P . Silencing or fueling metastasis with VEGF inhibitors: antiangiogenesis revisited. Cancer Cell. 2009; 15(3):167-70. DOI: 10.1016/j.ccr.2009.02.007. View

5.
Manicassamy S, Reizis B, Ravindran R, Nakaya H, Salazar-Gonzalez R, Wang Y . Activation of beta-catenin in dendritic cells regulates immunity versus tolerance in the intestine. Science. 2010; 329(5993):849-53. PMC: 3732486. DOI: 10.1126/science.1188510. View