Target intelligence / Profile preview

Proline-rich protein 11 (PRR11)

Target
PRR11
Molecular classification
Other (proline-rich protein), Transcription factor (due to zinc finger DNA-binding domain), Oncogene (functional molecular context in cancer)
01

Overview

Proline-rich protein 11 (PRR11) is a nuclear, proline-rich protein containing two proline-rich domains and a zinc finger DNA-binding motif, encoded at chromosome 17q22-23. PRR11 functions as a regulator of cell cycle progression, proliferation, migration, invasion, apoptosis, and autophagy. It is upregulated in diverse human cancers, promoting oncogenesis primarily through transcriptional and post-transcriptional effects on targets such as PTTG1 and by interacting with pathways including PI3K/AKT, Wnt/β-catenin, and E2F1. Overexpression of PRR11 is associated with poor prognosis and therapy resistance in several solid tumors, particularly breast, lung, ovarian, gastric, and colorectal cancers. PRR11 is increasingly recognized as an oncogenic driver, prognostic biomarker, and candidate therapeutic target, though no direct clinical inhibitors have been approved or reported as of the current literature.

Other names
Proline-rich protein 11PRR11FLJ11029transcription repressor of MHCII
02

Mechanism of action

Drugs targeting downstream or associated pathways (PI3K/AKT/mTOR, Wnt/β-catenin) may indirectly affect PRR11-positive cancer cell growth. Experimental gene silencing (e.g., siRNA knockdown) of PRR11 reduces proliferation and induces apoptosis in cancer cells.

03

Biological functions

Cell cycle progressionCell proliferationCell migrationCell invasionApoptosis regulationAutophagy regulationColony formationSignal transduction modulation via interactions with PI3K, E2F1, and Wnt/β-catenin pathways
04

Disease associations

Cancer (broadly, across multiple solid tumors: non-small cell lung cancer, breast cancer, ovarian cancer, gastric cancer, hepatocellular carcinoma, pancreatic cancer, colorectal cancer, and others)Cancer prognosis (biomarker for poor prognosis and therapy resistance)Chemoresistance (notably antiestrogen resistance in breast cancer)
05

Safety considerations

No specific safety concerns are reported for targeting PRR11 directly (no drugs developed), but challenges include: PRR11 is expressed in cell cycles and proliferation; inhibition may interfere with normal cellular proliferation.Potential for pleiotropic effects due to its modulation of multiple oncogenic pathways (PI3K, Wnt/β-catenin, etc.)
06

Interacting drugs

There are currently no clinically approved drugs that directly target PRR11. However, due to its role in PI3K and growth factor signaling, it is being researched as a potential therapeutic target; however, specific inhibitors are not reported in the peer-reviewed literature yet.
07

Biomarkers

PRR11 protein overexpression (immunohistochemistry) as a biomarker for cancer prognosis and disease stage, especially in ovarian and breast cancersPRR11 mRNA levels (gene expression profiling) in tumors for prognostic or monitoring purposes

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