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
. 2021 Jan 10;22(2):627.
doi: 10.3390/ijms22020627.

The Role of Noncoding RNAs in the Regulation of Anoikis and Anchorage-Independent Growth in Cancer

Affiliations
Review

The Role of Noncoding RNAs in the Regulation of Anoikis and Anchorage-Independent Growth in Cancer

Han Yeoung Lee et al. Int J Mol Sci. .

Abstract

Cancer is a global health concern, and the prognosis of patients with cancer is associated with metastasis. Multistep processes are involved in cancer metastasis. Accumulating evidence has shown that cancer cells acquire the capacity of anoikis resistance and anchorage-independent cell growth, which are critical prerequisite features of metastatic cancer cells. Multiple cellular factors and events, such as apoptosis, survival factors, cell cycle, EMT, stemness, autophagy, and integrins influence the anoikis resistance and anchorage-independent cell growth in cancer. Noncoding RNAs (ncRNAs), such as microRNAs (miRNAs) and long noncoding RNAs (lncRNAs), are dysregulated in cancer. They regulate cellular signaling pathways and events, eventually contributing to cancer aggressiveness. This review presents the role of miRNAs and lncRNAs in modulating anoikis resistance and anchorage-independent cell growth. We also discuss the feasibility of ncRNA-based therapy and the natural features of ncRNAs that need to be contemplated for more beneficial therapeutic strategies against cancer.

Keywords: anchorage-independent growth; anoikis; apoptosis; cancer; long noncoding RNA; metastasis; microRNA; noncoding RNA.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Oncogenic miRNAs (red) and their relevant target genes (black) facilitating anoikis resistance and anchorage-independent cell growth in cancer. It is described in Table 1 and Section 2.
Figure 2
Figure 2
Tumor-suppressive miRNAs (blue) and their relevant target genes (black) suppressing anoikis resistance and anchorage-independent cell growth in cancer. It is described in Table 2 and Section 3.
Figure 3
Figure 3
Oncogenic (red), tumor-suppressive (blue) lncRNAs, and miRNAs (black) that are affected by lncRNAs affecting anoikis and anchorage-independent cell growth in cancer. It is described in Table 3 and Section 4.

Similar articles

Cited by

References

    1. Kim Y.N., Koo K.H., Sung J.Y., Yun U.J., Kim H. Anoikis resistance: An essential prerequisite for tumor metastasis. Int. J. Cell Biol. 2012;2012:306879. doi: 10.1155/2012/306879. - DOI - PMC - PubMed
    1. Guadamillas M.C., Cerezo A., Del Pozo M.A. Overcoming anoikis—Pathways to anchorage-independent growth in cancer. J. Cell Sci. 2011;124:3189–3197. doi: 10.1242/jcs.072165. - DOI - PubMed
    1. Frisch S.M., Francis H. Disruption of epithelial cell-matrix interactions induces apoptosis. J. Cell Biol. 1994;124:619–626. doi: 10.1083/jcb.124.4.619. - DOI - PMC - PubMed
    1. Puthalakath H., Villunger A., O’Reilly L.A., Beaumont J.G., Coultas L., Cheney R.E., Huang D.C., Strasser A. Bmf: A proapoptotic BH3-only protein regulated by interaction with the myosin V actin motor complex, activated by anoikis. Science. 2001;293:1829–1832. doi: 10.1126/science.1062257. - DOI - PubMed
    1. Mailleux A.A., Overholtzer M., Schmelzle T., Bouillet P., Strasser A., Brugge J.S. Bim regulates apoptosis during mammary ductal morphogenesis, and its absence reveals alternative cell death mechanisms. Dev. Cell. 2007;12:221–234. doi: 10.1016/j.devcel.2006.12.003. - DOI - PMC - PubMed

LinkOut - more resources