Target intelligence / Profile preview

Long intergenic non-protein coding RNA 887 (LINC00887)

Target
LINC00887
Molecular classification
Other (Long non-coding RNA, lncRNA), Micropeptide-encoding lncRNA
01

Overview

LINC00887 is a long non-coding RNA (lncRNA) expressed in human cells, found to promote cell proliferation, migration, and metastasis in various cancers, including colorectal, lung, renal cell carcinoma, glioma, and papillary thyroid cancer[1][2][5][6]. It can function as a competing endogenous RNA, regulating miRNA degradation and acting through epigenetic modification pathways, such as GCN5-dependent H3K27 crotonylation and editing of ETS1 transcription[2]. Additionally, LINC00887 encodes a micropeptide (ACLY-BP) which stabilizes ATP citrate lyase (ACLY), thus promoting lipid deposition and providing acetyl-CoA for cellular metabolism[6]. It is upregulated in tumor tissue and associated with poor prognosis, cancer cell migration, and metastasis potential. LINC00887 and its functional protein product (ACLY-BP) are under investigation as biomarkers and therapeutic targets in cancer research[1][2][5][6].

Other names
ACLY-BPHEIRCCLINC02036linc-ATP13A4-8high-expressed in renal cell carcinomaACLY binding proteinLINC00887long intergenic non-protein coding RNA 2036
02

Mechanism of action

For therapeutic inhibition, likely action via RNA interference (siRNA, shRNA) targeting LINC00887 transcript or micropeptide inhibition[1][2][6].

03

Biological functions

Cell proliferationApoptosis regulationCell migration and invasionLipid metabolism and acetyl-CoA production (via ACLY-BP micropeptide)
04

Disease associations

Cancer (colorectal, renal cell carcinoma, lung, glioma, nasopharyngeal, papillary thyroid)Metastasis promotion in cancers
05

Safety considerations

No explicit safety concerns reportedChallenges inherent to lncRNA-targeting therapies include specificitydeliveryunintended regulation of non-target mRNAs or proteins
06

Biomarkers

Upregulated LINC00887H3K27cr (crotonylation) for colorectal cancer

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