Target intelligence / Profile preview

microRNA 557 (miR-557)

Target
miR-557
Molecular classification
MicroRNA, Non-coding RNA, Gene regulator, Other
01

Overview

microRNA 557 (miR-557) is a small non-coding RNA molecule consisting of approximately 19–22 nucleotides that regulates gene expression post-transcriptionally by binding to the 3'-untranslated region (3'-UTR) of target mRNAs, leading to mRNA degradation or translation repression. miR-557 is widely downregulated in various human cancers, including pancreatic, breast, gastric, and liver cancers. In pancreatic cancer, miR-557 functions as a tumor suppressor by inhibiting cellular proliferation, migration, and invasion, and promoting apoptosis. Mechanistically, miR-557 directly targets the epidermal growth factor receptor (EGFR) mRNA, reducing its protein expression. miR-557 is also involved in the regulation of other oncogenic pathways, such as IGF1 and mTOR signaling, in different cancer types. Outside of oncology, overexpression of miR-557 in mammalian cell lines has been shown to enhance recombinant protein production, indicating its pleiotropic regulatory effects. No approved drugs are currently known to target or mimic miR-557 directly, but it remains a promising research candidate for RNA-based cancer therapies[1][3]. **Notes** - miR-557 is not a receptor, enzyme, or transporter, but acts as a regulatory microRNA influencing a variety of disease processes through gene silencing. - It is considered a *therapeutic target* in cancer biology due to its documented tumor suppressor activity[1]. - No approved diagnostic or therapeutic agents specifically targeting miR-557 are listed; it is a potential biomarker for pancreatic and other cancers[1]. - There is no evidence the entry is incorrect or misnamed; aliases are well-attested in the literature[1][3].

Other names
hsa-miR-557MIRN557MIR557hsa-mir-557
02

Mechanism of action

Silencing target mRNA translation (e.g., EGFR), mRNA degradation (via 3'-UTR binding)

03

Biological functions

Post-transcriptional gene silencingRegulation of mRNA stabilityApoptosisCell proliferationCell migrationCell invasionTumor suppression
04

Disease associations

Cancerpancreatic cancerliposarcomahepatocellular carcinomatriple-negative breast cancergastric cancer
05

Safety considerations

No prominent direct safety concerns describedtherapeutic delivery and specificity for RNA therapeutics are general challenges in the field
06

Biomarkers

Lower miR-557 expression as a marker of pancreatic cancerlow level in other cancers

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