Target intelligence / Profile preview

FMR1 neighbor protein (FMR1NB)

Target
FMR1NB
Molecular classification
Other (Cancer/testis antigen; protein-coding gene, possible surface/cytoplasmic localization)
01

Overview

FMR1 neighbor protein (FMR1NB) is a cancer/testis antigen composed of 255 amino acids and encoded by a gene on chromosome X. It has restricted expression in normal tissues (mainly testis/placenta), but is upregulated in diverse cancers. The protein acts as a positive regulator of mitosis, participating in microtubule nucleation and spindle anchoring during cell division. Its aberrant expression in cancer promotes cell proliferation and invasiveness. Identified using serological analysis (SEREX), FMR1NB/NY-SAR-35 is the focus of experimental peptide vaccine programs, leveraging its immunogenic epitopes for anti-cancer immunotherapy. The potential for biomarker-based patient selection and targeted therapy is under investigation

Other names
CT37FLJ25736NY-SAR-35Sarcoma antigen NY-SAR-35Cancer/testis antigen 37NYSAR35
02

Mechanism of action

Proposed immunotherapy mechanism: induction of specific cytotoxic T cell responses via MHC-I and MHC-II presentation of FMR1NB-derived epitopes

03

Biological functions

Cell proliferationCell cycle regulation (positive regulator of mitosis)Microtubule nucleation and spindle anchoring
04

Disease associations

Cancer (melanoma, sarcoma, lung, breast, bladder, esophageal, ovarian)
05

Safety considerations

Cancer/testis antigens like FMR1NB have restricted expression mainly in immune-privileged sites (testis/placenta), but off-target immune responses remain a theoretical risk (autoimmunity or infertility).Potential allergenicity, toxicity, or unwanted immune responses to therapeutic epitopes must be evaluated in preclinical and clinical studies
06

Interacting drugs

None currently clinically approved; experimental cancer vaccines have been developed targeting NY-SAR-35/FMR1NB epitopes
07

Biomarkers

Tumor tissue expression of FMR1NB/NY-SAR-35 (may be used for patient selection in cancer immunotherapy trials)

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