Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Apr;23(4):121.
doi: 10.3892/ol.2022.13241. Epub 2022 Feb 14.

Research progress on RNA-binding proteins in breast cancer

Affiliations
Review

Research progress on RNA-binding proteins in breast cancer

Wenzhu Zhang et al. Oncol Lett. 2022 Apr.

Abstract

Breast cancer is the most common malignancy among women, and the abnormal regulation of gene expression serves an important role in its occurrence and development. However, the molecular mechanisms underlying gene expression are highly complex and heterogeneous, and RNA-binding proteins (RBPs) are among the key regulatory factors. RBPs bind targets in an environment-dependent or environment-independent manner to influence mRNA stability and the translation of genes involved in the formation, progression, metastasis and treatment of breast cancer. Due to the growing interest in these regulators, the present review summarizes the most influential studies concerning RBPs associated with breast cancer to elucidate the role of RBPs in breast cancer and to assess how they interact with other key pathways to provide new molecular targets for the diagnosis and treatment of breast cancer.

Keywords: RNA-binding protein; breast cancer; research progress.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Figure 1.
Figure 1.
eIF4E, its target genes and its modulators in cellular pathways. Arrows indicate activation.
Figure 2.
Figure 2.
HuR, its target genes and its modulators in cellular pathways. Arrows indicate activation and blunted lines indicate inhibition.
Figure 3.
Figure 3.
IMPs, their target genes and their modulators in cellular pathways. Arrows indicate activation and blunted lines indicate inhibition.
Figure 4.
Figure 4.
LIN28, its target genes and its modulators in cellular pathways. Arrows indicate activation and blunted lines indicate inhibition.
Figure 5.
Figure 5.
MSI, their target genes and their modulators in cellular pathways. Arrows indicate activation and blunted lines indicate inhibition.
Figure 6.
Figure 6.
RBM38, its target genes and its modulators in cellular pathways. Arrows indicate activation and blunted lines indicate inhibition.
Figure 7.
Figure 7.
SAM68, its target genes and its modulators in cellular pathways. Arrows indicate activation and blunted or crossed-out lines indicate inhibition.

Similar articles

Cited by

References

    1. Smith RA, Andrews KS, Brooks D, Fedewa SA, Manassaram-Baptiste D, Saslow D, Wender RC. Cancer screening in the United States, 2019: A review of current American cancer society guidelines and current issues in cancer screening. CA Cancer J Clin. 2019;69:184–210. doi: 10.3322/caac.21557. - DOI - PubMed
    1. Skibinski A, Kuperwasser C. The origin of breast tumor heterogeneity. Oncogene. 2015;34:5309–5316. doi: 10.1038/onc.2014.475. - DOI - PMC - PubMed
    1. Wang L, Gallo KA, Conrad SE. Targeting mixed lineage kinases in ER-positive breast cancer cells leads to G2/M cell cycle arrest and apoptosis. Oncotarget. 2013;4:1158–1171. doi: 10.18632/oncotarget.1093. - DOI - PMC - PubMed
    1. Sommer S, Fuqua SA. Estrogen receptor and breast cancer. Semin Cancer Biol. 2001;11:339–352. doi: 10.1006/scbi.2001.0389. - DOI - PubMed
    1. Slamon D, Leyland-Jones B, Shak S, Fuchs H, Paton V, Bajamonde A, Fleming T, Eiermann W, Wolter J, Pegram M, et al. Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. N Engl J Med. 2001;344:783–792. doi: 10.1056/NEJM200103153441101. - DOI - PubMed