Target intelligence / Profile preview

Ribosomal protein SA pseudogene 52 (RPSAP52)

Target
RPSAP52
Molecular classification
Long non-coding RNA (lncRNA), Pseudogene transcript, Competing endogenous RNA (ceRNA)
01

Overview

Ribosomal protein SA pseudogene 52 (RPSAP52) is a long non-coding RNA recognized for its oncogenic properties across various human cancers. It is a transcribed pseudogene running antisense to HMGA2, influencing both nuclear and cytoplasmic gene regulation. RPSAP52 acts as a competing endogenous RNA, sequestering miRNAs to derepress oncogenes, and also interacts with RNA-binding proteins (notably IGF2BP2) to facilitate the translation of target mRNAs such as HMGA2 and LIN28B. Its overexpression leads to cancer cell proliferation, enhanced stemness, and poor clinical outcomes. Additionally, RPSAP52 may play a role in non-cancer diseases like renal failure by modulating gene expression under hypoxic conditions. RPSAP52 is being explored as a prognostic and diagnostic biomarker and as a candidate for experimental RNA-targeting therapies, but is not an established direct therapeutic target[1][2][3][5].

Other names
RPSAP52Ribosomal protein SA pseudogene 52
02

Mechanism of action

Not applicable for approved drugs. In research, antisense oligonucleotides (e.g., GapmeRs) have been used to knock down RPSAP52, leading to reduced tumor growth[5].

03

Biological functions

Regulation of gene expression at transcriptional and post-transcriptional levelsCompeting endogenous RNA activity: sequesters specific microRNAs (miR-15a, miR-15b, miR-16, miR-423-5p)Positive regulation of HMGA2, HMGA1, and TGF-β1 gene and protein expressionFacilitation of cell cycle progression (G1-S transition)Enhancement of cancer cell proliferation, survival, and stemnessModulation of cell differentiation and myogenesisInteraction with RNA-binding proteins (notably IGF2BP2/IMP2)
04

Disease associations

Cancer (notably pituitary adenoma, glioblastoma, sarcoma, ovarian cancer, rhabdomyosarcoma, and more)Poor prognosis and cancer progression biomarkerRenal failure (potential protective role in proximal tubular cells under hypoxia)
05

Safety considerations

No established clinical safety concerns, as RPSAP52 is not a therapeutic target in current clinical useAntisense knockdown strategies are experimental, with unknown clinical safety profile
06

Biomarkers

RPSAP52 expression level in tumors (high levels predict poor prognosis in various cancers, especially glioblastoma, sarcoma, ovarian cancer)HMGA2 expression (functionally linked biomarker)TGF-β1 expression (positively regulated by RPSAP52 in glioblastoma)

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