Related Experiment Video
Updated: Oct 4, 2026

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
Characterization of a novel gene, STAG1/PMEPA1, upregulated in renal cell carcinoma and other solid tumors
F K Rae1, J D Hooper, D L Nicol
1Centre for Molecular Biotechnology, School of Life Sciences, Queensland University of Technology, Brisbane, Australia.
Abstract:
Using differential display-polymerase chain reaction, we identified a novel gene sequence, designated solid tumor-associated gene 1 (STAG1), that is upregulated in renal cell carcinoma (RCC). The full-length cDNA (4839 bp) encompassed the recently reported androgen-regulated prostatic cDNA PMEPA1, and so we refer to this gene as STAG1/PMEPA1. Two STAG1/PMEPA1 mRNA transcripts of approximately 2.7 and 5 kb, with identical coding regions but variant 3' untranslated regions, were predominantly expressed in normal prostate tissue and at lower levels in the ovary. The expression of this gene was upregulated in 87% of RCC samples and also was upregulated in stomach and rectal adenocarcinomas. In contrast, STAG1/PMEPA1 expression was barely detectable in leukemia and lymphoma samples. Analysis of expressed sequence tag databases showed that STAG1/PMEPA1 also was expressed in pancreatic, endometrial, and prostatic adenocarcinomas. The STAG1/PMEPA1 cDNA encodes a 287-amino-acid protein containing a putative transmembrane domain and motifs that suggest that it may bind src homology 3- and tryptophan tryptophan domain-containing proteins. This protein shows 67% identity to the protein encoded by the chromosome 18 open reading frame 1 gene. Translation of STAG1/PMEPA1 mRNA in vitro showed two products of 36 and 39 kDa, respectively, suggesting that translation may initiate at more than one site. Comparison to genomic clones showed that STAG1/PMEPA1 was located on chromosome 20q13 between microsatellite markers D20S183 and D20S173 and spanned four exons and three introns. The upregulation of this gene in several solid tumors indicated that it may play an important role in tumorigenesis.
Insights
A novel gene, solid tumor-associated gene 1 (STAG1), is upregulated in renal cell carcinoma and other solid tumors, suggesting a role in cancer development.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Renal cell carcinoma (RCC) is a significant health concern.
- Identification of novel cancer-associated genes is crucial for understanding tumorigenesis.
Purpose of the Study:
- To identify and characterize novel genes involved in solid tumor development.
- To investigate the expression patterns of a newly identified gene in various cancer types.
Main Methods:
- Differential display-polymerase chain reaction (DD-PCR) for gene discovery.
- Full-length cDNA sequencing and mRNA transcript analysis.
- Gene expression profiling in tumor and normal tissues.
- Bioinformatic analysis of expressed sequence tag databases.
- Protein analysis and genomic localization.
Main Results:
- A novel gene, solid tumor-associated gene 1 (STAG1), was identified and found to be upregulated in 87% of RCC samples.
- STAG1/PMEPA1 expression was also elevated in stomach, rectal, pancreatic, endometrial, and prostatic adenocarcinomas.
- Expression was significantly lower in leukemia and lymphoma.
- Two mRNA transcripts (2.7 and 5 kb) and two protein products (36 and 39 kDa) were identified.
- The gene is located on chromosome 20q13 and encodes a protein with a putative transmembrane domain.
Conclusions:
- STAG1/PMEPA1 upregulation in multiple solid tumors suggests its potential role in tumorigenesis.
- This gene represents a potential biomarker and therapeutic target for various cancers.
Related Concept Videos
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Abnormal Proliferation
Cell Specific Gene Expression