Target intelligence / Profile preview

FKBP prolyl isomerase 9 pseudogene 1 (FKBP9P1)

Target
FKBP9P1
Molecular classification
Other (long non-coding RNA, pseudogene; not a classical protein target, but part of non-coding RNA regulatory networks)
01

Overview

FKBP prolyl isomerase 9 pseudogene 1 (FKBP9P1) is classified as a long non-coding RNA pseudogene related to the FKBP family, but does not encode a functional protein. Recent studies implicate FKBP9P1 in the progression of head and neck squamous cell carcinoma, where its high expression correlates with increased cell proliferation, migration, invasion, and a poor patient prognosis. Mechanistically, FKBP9P1 appears to regulate cancer cell biology through effects on the PI3K/AKT signaling pathway, and silencing FKBP9P1 suppresses these tumorigenic phenotypes in vitro. This suggests FKBP9P1 may be a promising diagnostic and prognostic marker, as well as a potential molecular target for future therapeutics in oncology. Unlike classical FKBP family proteins, FKBP9P1 does not function as an enzyme, receptor, or protein chaperone, and there are no known direct chemical modulators. It is not a canonical therapeutic target but does function as a disease-associated regulatory lncRNA. Key limitations: FKBP9P1 is commonly mischaracterized as a protein, but is a non-coding RNA pseudogene; therapeutic targeting remains theoretical, with active research focused on its role in cancer biology rather than direct drug modulation.

Other names
Putative FK506-binding protein 9-like proteinFKBP9P1FKBP9LMGC20531FK506-binding protein 9-like protein pseudogene
02

Biological functions

Cell proliferation (positive regulation in HNSCC)Cell migration and invasion (positive regulation in HNSCC)PI3K/AKT pathway regulation (influences activity when silenced in cancer cells)
03

Disease associations

Cancer (specifically implicated in head and neck squamous cell carcinoma, promoting progression and invasiveness; high levels predict poor prognosis)
04

Biomarkers

High FKBP9P1 expression serves as a prognostic biomarker for advanced stage and poor survival in patients with HNSCC

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