» Articles » PMID: 26762415

Lin28: an Emerging Important Oncogene Connecting Several Aspects of Cancer

Overview
Journal Tumour Biol
Publisher Sage Publications
Specialty Oncology
Date 2016 Jan 15
PMID 26762415
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

RNA-binding protein Lin28 was originally found as a heterochronic gene which played a significant role in the development of Caenorhabditis elegans. The tumor suppressor let-7 is a downstream target of Lin28, which has a wide variety of target genes which are involved in many aspects of cellular activities. By inhibition of let-7 and directly binding the target RNAs, Lin28 plays an important role in different biological and pathological processes including differentiation, metabolism, proliferation, pluripotency, and tumorigenesis. Overexpression of Lin28 has been reported in several kinds of cancers and is correlated with poor outcomes. It has been shown that Lin28 could affect the progression of cancers in several ways, such as promoting proliferation, increasing glucose metabolism, and inducing epithelial-mesenchymal transition (EMT) and cancer stem cells. Decrease of Lin28 expression or reactivation of let-7 in cancer cells could induce a reverse effect, indicating their therapeutic values in developing novel strategies for cancer treatment. Here, we will overview the regulatory mechanisms and functions of Lin28 in cancers.

Citing Articles

Nephron-Specific Overexpression Triggers Severe Inflammatory Response and Kidney Damage.

Futorian A, Armon L, Waldman Ben-Asher H, Shoval I, Hazut I, Munitz A Int J Biol Sci. 2024; 20(10):4044-4054.

PMID: 39113694 PMC: 11302891. DOI: 10.7150/ijbs.97434.


Advances of Genome Editing with CRISPR/Cas9 in Neurodegeneration: The Right Path towards Therapy.

Klinkovskij A, Shepelev M, Isaakyan Y, Aniskin D, Ulasov I Biomedicines. 2023; 11(12).

PMID: 38137554 PMC: 10741756. DOI: 10.3390/biomedicines11123333.


Mutual connected IL-6, EGFR and LIN28/Let7-related mechanisms modulate PD-L1 and IGF upregulation in HNSCC using immunotherapy.

Li J, Xiao Y, Yu H, Jin X, Fan S, Liu W Front Oncol. 2023; 13:1140133.

PMID: 37124491 PMC: 10130400. DOI: 10.3389/fonc.2023.1140133.


LIN28B Enhanced STAT3 Signaling Regulates Inflammatory Response and Chemotherapeutic Resistance in Cholangiocytes.

Puthdee N, Khramchantuk S, Nuwongsri P Asian Pac J Cancer Prev. 2021; 22(11):3671-3678.

PMID: 34837926 PMC: 9068185. DOI: 10.31557/APJCP.2021.22.11.3671.


The LIN28B/TGF-β/TGFBI feedback loop promotes cell migration and tumour initiation potential in cholangiocarcinoma.

Puthdee N, Sriswasdi S, Pisitkun T, Ratanasirintrawoot S, Israsena N, Tangkijvanich P Cancer Gene Ther. 2021; 29(5):445-455.

PMID: 34548635 PMC: 9113936. DOI: 10.1038/s41417-021-00387-5.


References
1.
Wang L, Zhang L, Wu J, Xu S, Xu Y, Li D . IL-1β-mediated repression of microRNA-101 is crucial for inflammation-promoted lung tumorigenesis. Cancer Res. 2014; 74(17):4720-30. DOI: 10.1158/0008-5472.CAN-14-0960. View

2.
Li Y, VandenBoom 2nd T, Kong D, Wang Z, Ali S, Philip P . Up-regulation of miR-200 and let-7 by natural agents leads to the reversal of epithelial-to-mesenchymal transition in gemcitabine-resistant pancreatic cancer cells. Cancer Res. 2009; 69(16):6704-12. PMC: 2727571. DOI: 10.1158/0008-5472.CAN-09-1298. View

3.
Hu Q, Peng J, Liu W, He X, Cui L, Chen X . Lin28B is a novel prognostic marker in gastric adenocarcinoma. Int J Clin Exp Pathol. 2014; 7(8):5083-92. PMC: 4152071. View

4.
Li N, Zhong X, Lin X, Guo J, Zou L, Tanyi J . Lin-28 homologue A (LIN28A) promotes cell cycle progression via regulation of cyclin-dependent kinase 2 (CDK2), cyclin D1 (CCND1), and cell division cycle 25 homolog A (CDC25A) expression in cancer. J Biol Chem. 2012; 287(21):17386-17397. PMC: 3366838. DOI: 10.1074/jbc.M111.321158. View

5.
Wilbert M, Huelga S, Kapeli K, Stark T, Liang T, Chen S . LIN28 binds messenger RNAs at GGAGA motifs and regulates splicing factor abundance. Mol Cell. 2012; 48(2):195-206. PMC: 3483422. DOI: 10.1016/j.molcel.2012.08.004. View