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Published on: May 10, 2024
KIAA1324 Suppresses Gastric Cancer Progression by Inhibiting the Oncoprotein GRP78
Jin Muk Kang1, Sujin Park1, Staci Jakyong Kim2
1CHA Cancer Institute, College of Life Science, CHA University, Seongnam City, Republic of Korea.
Abstract:
Recent advances in genome and transcriptome analysis have contributed to the identification of many potential cancer-related genes. Furthermore, biological and clinical investigations of the candidate genes provide us with a better understanding of carcinogenesis and development of cancer treatment. Here, we report a novel role of KIAA1324 as a tumor suppressor in gastric cancer. We observed that KIAA1324 was downregulated in most gastric cancers from transcriptome sequencing data and found that histone deacetylase was involved in the suppression of KIAA1324. Low KIAA1324 levels were associated with poor prognosis in gastric cancer patients. In the xenograft model, KIAA1324 significantly reduced tumor formation of gastric cancer cells and decreased development of preformed tumors. KIAA1324 also suppressed proliferation, invasion, and drug resistance and induced apoptosis in gastric cancer cells. Through protein interaction analysis, we identified GRP78 (glucose-regulated protein 78 kDa) as a KIAA1324-binding partner. KIAA1324 blocked oncogenic activities of GRP78 by inhibiting GRP78-caspase-7 interaction and suppressing GRP78-mediated AKT activation, thereby inducing apoptosis. In conclusion, our study reveals a tumor suppressive role of KIAA1324 via inhibition of GRP78 oncoprotein activities and provides new insight into the diagnosis and treatment of gastric cancer.
Insights
KIAA1324 acts as a tumor suppressor in gastric cancer by downregulating oncogenic GRP78. Low KIAA1324 levels correlate with poor prognosis, suggesting its potential as a therapeutic target.
Area of Science:
- Genomics and Molecular Oncology
- Cancer Biology
Background:
- Genome and transcriptome analyses identify cancer-related genes.
- Understanding gene function aids in comprehending carcinogenesis and cancer treatment.
Purpose of the Study:
- To investigate the role of KIAA1324 in gastric cancer.
- To elucidate the molecular mechanisms underlying KIAA1324's function.
Main Methods:
- Transcriptome sequencing to identify gene expression patterns.
- In vivo xenograft models to assess tumor formation.
- Protein interaction analysis to identify binding partners.
- Cellular assays for proliferation, invasion, apoptosis, and drug resistance.
Main Results:
- KIAA1324 is downregulated in gastric cancer, linked to poor prognosis.
- KIAA1324 suppresses tumor formation, proliferation, invasion, and drug resistance.
- KIAA1324 interacts with GRP78, inhibiting its oncogenic activities and inducing apoptosis.
- Histone deacetylase is implicated in KIAA1324 suppression.
Conclusions:
- KIAA1324 functions as a tumor suppressor in gastric cancer.
- KIAA1324 inhibits GRP78 oncoprotein activity, leading to apoptosis.
- KIAA1324 presents a potential target for gastric cancer diagnosis and therapy.
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