New targets in the fight against pancreatic cancer
November 10, 2022
Researchers from Tokyo Medical and Dental University (TMDU) uncover an important relationship between two genes critical to pancreatic cancer patient prognosis
Tokyo, Japan – Pancreatic cancer remains one of the deadliest malignancies worldwide. Since five-year survival rate for pancreatic ductal adenocarcinoma (PDAC) is only about 3% in patients, PDAC is very difficult to treat with surgery worldwide. To develop novel treatment methods, the biology of PDAC at the molecular level needs to be better understood.
In a recent article published in Cancer Science, researchers from Tokyo Medical and Dental University (TMDU) have identified a new target gene that has strong clinical implications in PDAC cases.
Previous studies have demonstrated that cancer cells express high levels of a special enzyme—histone H3K4 methyltransferase—that is encoded by SETD1A gene. This enzyme regulates gene expression by adding a methyl chemical group to histone proteins (essential structural components of chromatin) of specific target genes through a process called methylation. However, the mechanism causing overexpression of this enzyme and its effect on cancer cells remain unclear. Following histone methylation, the target genes become active. This is especially significant if SETD1A target genes can support cancer development and progression. Therefore, researchers from TMDU became interested in understanding the role of SETD1A overexpression in PDAC.
“Although previous work has shown that SETD1A is overexpressed in various cancer, such as gastric and lung cancer, the specific molecular events of SETD1A are not understood in PDAC,” says lead author Takeshi Ishii. “SETD1A target genes in PDAC have also not yet been identified.”
The researchers observed high levels of SETD1A expression in 51.4% of the human PDAC samples they analyzed. They also determined that SETD1A was an independent prognostic factor for disease-free survival, meaning that after tumor resection, patients with high SETD1A levels live in a disease-free state for a shorter duration than those with low SETD1A levels. These results demonstrate the clinical importance of SETD1A expression in PDAC.
Then, they used artificially cultured PDAC cells to examine how changing SETD1A expression would affect cell behavior. When they overexpressed SETD1A levels, both cell growth and cell migration ability increased. In another set of PDAC cells, researchers used molecular techniques to interfere with SETD1A expression and then analyzed other genes that were affected by this. “Using a technique called RNA sequencing, we examined overall gene expression after knocking down SETD1A and found that another gene known as RUVBL1 was expressed at lower levels,” explains senior author Shinji Tanaka.
Further work suggested that SETD1A can methylate histones near the RUVBL1 gene and activate its gene expression. Knocking down RUVBL1 expression in PDAC cells had similar biological effects to those observed earlier with SETD1A interference. “Analysis of survival rates revealed that PDAC patients with high SETD1A and RUVBL1 levels had poorer overall survival, suggesting that their co-expression is an important prognostic biomarker for this cancer,” says Takeshi Ishii.
The study results provide deeper insights into the significance of SETD1A and RUVBL1 expression in PDAC and may offer crucial details to help clinicians with critical treatment decisions for patients suffering from this serious disease.
In a recent article published in Cancer Science, researchers from Tokyo Medical and Dental University (TMDU) have identified a new target gene that has strong clinical implications in PDAC cases.
Previous studies have demonstrated that cancer cells express high levels of a special enzyme—histone H3K4 methyltransferase—that is encoded by SETD1A gene. This enzyme regulates gene expression by adding a methyl chemical group to histone proteins (essential structural components of chromatin) of specific target genes through a process called methylation. However, the mechanism causing overexpression of this enzyme and its effect on cancer cells remain unclear. Following histone methylation, the target genes become active. This is especially significant if SETD1A target genes can support cancer development and progression. Therefore, researchers from TMDU became interested in understanding the role of SETD1A overexpression in PDAC.
“Although previous work has shown that SETD1A is overexpressed in various cancer, such as gastric and lung cancer, the specific molecular events of SETD1A are not understood in PDAC,” says lead author Takeshi Ishii. “SETD1A target genes in PDAC have also not yet been identified.”
The researchers observed high levels of SETD1A expression in 51.4% of the human PDAC samples they analyzed. They also determined that SETD1A was an independent prognostic factor for disease-free survival, meaning that after tumor resection, patients with high SETD1A levels live in a disease-free state for a shorter duration than those with low SETD1A levels. These results demonstrate the clinical importance of SETD1A expression in PDAC.
Then, they used artificially cultured PDAC cells to examine how changing SETD1A expression would affect cell behavior. When they overexpressed SETD1A levels, both cell growth and cell migration ability increased. In another set of PDAC cells, researchers used molecular techniques to interfere with SETD1A expression and then analyzed other genes that were affected by this. “Using a technique called RNA sequencing, we examined overall gene expression after knocking down SETD1A and found that another gene known as RUVBL1 was expressed at lower levels,” explains senior author Shinji Tanaka.
Further work suggested that SETD1A can methylate histones near the RUVBL1 gene and activate its gene expression. Knocking down RUVBL1 expression in PDAC cells had similar biological effects to those observed earlier with SETD1A interference. “Analysis of survival rates revealed that PDAC patients with high SETD1A and RUVBL1 levels had poorer overall survival, suggesting that their co-expression is an important prognostic biomarker for this cancer,” says Takeshi Ishii.
The study results provide deeper insights into the significance of SETD1A and RUVBL1 expression in PDAC and may offer crucial details to help clinicians with critical treatment decisions for patients suffering from this serious disease.
The molecular mechanism and clinical significance of SETDA1 overexpression in pancreatic cancer
Top, SETD1A, directly recruited to the RUVBL1 promoter, enhances RUVBL1 gene expression by increasing H3K4me3 levels in pancreatic cancer cells. Bottom, High co-expression of SETD1A and RUVBL1 can predict worse prognosis than others.
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The article, “Identification of a novel target of SETD1A histone methyltransferase and the clinical significance in pancreatic cancer,” was published in Cancer Science at DOI:10.1111/cas.15615
Summary
Tokyo Medical and Dental University (TMDU) researchers examined pancreatic ductal adenocarcinoma (PDAC) cases and found increased expression of a gene called SETD1A. Elevated levels of SETD1A enhanced PDAC cell growth and migration, while interfering with its expression resulted in lower levels of RUVBL1, which they found was a SETD1A target gene. PDAC patients with high expression of both SETD1A and RUVBL1 had poorer overall survival. This study may help clinicians make important decisions for PDAC treatment.
Journal Article
JOURNAL：Cancer Science
TITLE：Identification of a novel target of SETD1A histone methyltransferase and the clinical significance in pancreatic cancer
DOI：https://doi.org/10.1111/cas.15615
TITLE：Identification of a novel target of SETD1A histone methyltransferase and the clinical significance in pancreatic cancer
DOI：https://doi.org/10.1111/cas.15615
Correspondence to
Shinji TANAKA,M.D., Ph.D., Professor
Yoshimitsu Akiyama, Junior Associate Professor
Department of Molecular Oncology,
Graduated School of Medical and Dental Sciences,
Tokyo Medical and Dental University(TMDU)
E-mail：tanaka.monc(at)tmd.ac.jp
E-mail：yakiyama.monc(at)tmd.ac.jp
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