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Shiuan Chen, Ph.D. - Laboratory and Research Focus

Breast Cancer Translational Research
 
Dr. Shiuan Chen was one of the three investigators who originally isolated the full-length human aromatase cDNA clones. Aromatase is an enzyme that converts androgen to estrogen. Aromatase inhibitors (AIs) are important drugs to treat estrogen-dependent breast cancer. Approximately 60% of premenopausal and 75% of postmenopausal breast cancer patients have estrogen-dependent carcinomas.
 
Since aromatase is the enzyme responsible for the synthesis of estrogen, and estrogen can have a major effect in the development of breast cancer, an abnormal expression of aromatase in breast cancer cells and/or surrounding adipose stromal cells may have a significant influence on breast tumor development and growth in cancer patients. Aromatase is expressed at higher levels in human breast cancer tissue than in normal breast tissue, as measured by various biochemical assays. During the last ten years, AIs have been demonstrated to be superior to tamoxifen for the treatment of hormonal dependent breast cancer. While this new generation of aromatase inhibitors is shown to be useful in the treatment of hormonal responsive breast cancer, resistance to such endocrine therapy still develops. Through collaboration with Yate-Ching Yuan, Ph.D., (Bioinformatics), we are carrying out gene expression array experiments on AI-responsive as well as resistant cell lines that have been generated in our laboratory. We plan to identify and functionally confirm the roles of genes involved in resistance.
 
It is hypothesized that these studies will produce valuable molecular information regarding the mechanisms of AI resistance, and the information will help design approaches to reduce resistance and improve the efficacy of AI treatments of breast cancer. Furthermore, our research has led to the identification of a HDAC inhibitor: LBH589 is a selective aromatase expression suppressor and a drug to inhibit the development of AI resistance. After reviewing the results generated from our preclinical studies, we have started working with Joanne Mortimer, M.D., George Somlo, M.D. and Thehang Luu, M.D., (Medical Oncology) in the design of new therapeutic approaches to treat AI resistant breast cancer. Hormone Diagram
 
We are also conducting research to determine how environmental chemicals modulate the activity and expression of aromatase in human tissue. Experiments are being conducted to provide a molecular and mechanistic basis as to how phytochemicals and organochlorine compounds affect estrogen biosynthesis (i.e., aromatase function) in women. Research from Dr. Chen's and other laboratories have revealed that ER, aromatase, and ERRα are key players in breast cancer promotion and in cancer recurrence following endocrine treatment. Furthermore, proof-of-concept studies have revealed that these proteins are targets of endocrine disruptors. Based on these observations, we hypothesize that environmental chemicals will play critical roles in modulating breast cancer through ER, aromatase, and ERRα. The goal of this research is to develop screening assays for identifying and testing chemicals with relevance to known and suspected causes of estrogen-dependent breast cancer. Our collaborators include Richard Yip, Ph.D. (High Throughput Screening Core), Charles Wang, Ph.D. (Functional Genomics Core), Yate-Ching Yuan, Ph.D. (Bioinformatics Core), Christina Teng, Ph.D. (National Institute of Environmental Health Sciences), and Sandra Finestone, Psy.D. (Hope Wellness Center, Costa Mesa, CA).
 
 
Chemoprevention Research Program

Since the summer of 2004, Dr. Chen and 27 other investigators have initiated an effort to develop a chemoprevention research program at City of Hope. Through biweekly meetings, these Beckman researchers and clinicians exchange research information and ideas. Four research areas have recently been chosen to focus on. The immediate goal is to generate preliminary results in these new target areas that will lead to the development of multidiscipline translational chemoprevention research projects at our institution.

Our laboratory has found that grapes, mushrooms and pomegranate contain chemicals that can suppress aromatase activity. Therefore, a diet that includes grapes, mushrooms and pomegranate would be considered preventative against breast cancer. We are purifying and characterizing these natural anti-aromatase chemicals and evaluating their in vivo effects using animal experiments. The active chemicals in grapes have been found to be procyanidin dimers that are present at high concentrations in grape seeds. Melanie Palomares, M.D., (Population Sciences), Jeffrey Weitzel, M.D., (Clinical Cancer Genetics), Tim Synold, Pharm.D., (Experimental Therapeutics) and this laboratory have collaborated and initiated a grape seed extract clinical trial and a mushroom clinical trial based on the chemoprevention studies against breast cancer performed in our laboratory.

Furthermore, we have found that mushrooms contain chemicals that act as inhibitors of steroid 5-alpha reductase. Androgen plays a critical role in prostate cancer development. In the prostate, testosterone (an androgen) is converted to dihydrotestosterone (DHT), an androgen that is even more potent than testosterone. This conversion is catalyzed by the enzyme steroid 5-alpha reductase. An elevation of the steroid 5-alpha reductase activity in the prostate may cause benign prostate hyperplasia (a common problem in older men) and also promote the growth of prostate cancer. Animal experiments have been performed to evaluate the use of these phytochemicals as drugs in the prevention and/or treatment of prostate cancer. One clinical trial designed, based Dr. Chen's findings, is being carried out at City of Hope with Przemyslaw Twardowski, M.D. (Medical Oncology). A recent study in the Chen laboratory has revealed that the intake of mushrooms may reduce the incidence of metabolic diseases such as fatty liver and insulin resistance.

In addition, experiments have been carried out to show that blueberry contains phytochemicals that can suppress the proliferation and migration of triple negative breast cancer in cell culture and animals. Efforts are being made to initiate a blueberry clinical trial at City of Hope.
 
For more information on Dr. Chen, please click here.

Shiuan Chen, Ph.D. Lab Members

Hei (Jason) Chan, B.S.
Graduate Student
626-256-HOPE (4673), Ext. 63056
 
Zhike Chen, Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 6506
 
Masaya Kai, Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 60562
 
Noriko Kanaya, Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 65062
 
Karineh Petrossian, M.S.
Graduate Student
626-256-HOPE (4673), Ext. 65062
 
Yuan-Zhong Wang, Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 6305
 
Cynthie Wong , Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 63056
 
Dujin Zhou, Ph.D.
Associate Research Scientist
626-256-HOPE (4673), Ext. 64908
 

Chen, Shiuan, Ph.D.

Shiuan Chen, Ph.D. - Laboratory and Research Focus

Breast Cancer Translational Research
 
Dr. Shiuan Chen was one of the three investigators who originally isolated the full-length human aromatase cDNA clones. Aromatase is an enzyme that converts androgen to estrogen. Aromatase inhibitors (AIs) are important drugs to treat estrogen-dependent breast cancer. Approximately 60% of premenopausal and 75% of postmenopausal breast cancer patients have estrogen-dependent carcinomas.
 
Since aromatase is the enzyme responsible for the synthesis of estrogen, and estrogen can have a major effect in the development of breast cancer, an abnormal expression of aromatase in breast cancer cells and/or surrounding adipose stromal cells may have a significant influence on breast tumor development and growth in cancer patients. Aromatase is expressed at higher levels in human breast cancer tissue than in normal breast tissue, as measured by various biochemical assays. During the last ten years, AIs have been demonstrated to be superior to tamoxifen for the treatment of hormonal dependent breast cancer. While this new generation of aromatase inhibitors is shown to be useful in the treatment of hormonal responsive breast cancer, resistance to such endocrine therapy still develops. Through collaboration with Yate-Ching Yuan, Ph.D., (Bioinformatics), we are carrying out gene expression array experiments on AI-responsive as well as resistant cell lines that have been generated in our laboratory. We plan to identify and functionally confirm the roles of genes involved in resistance.
 
It is hypothesized that these studies will produce valuable molecular information regarding the mechanisms of AI resistance, and the information will help design approaches to reduce resistance and improve the efficacy of AI treatments of breast cancer. Furthermore, our research has led to the identification of a HDAC inhibitor: LBH589 is a selective aromatase expression suppressor and a drug to inhibit the development of AI resistance. After reviewing the results generated from our preclinical studies, we have started working with Joanne Mortimer, M.D., George Somlo, M.D. and Thehang Luu, M.D., (Medical Oncology) in the design of new therapeutic approaches to treat AI resistant breast cancer. Hormone Diagram
 
We are also conducting research to determine how environmental chemicals modulate the activity and expression of aromatase in human tissue. Experiments are being conducted to provide a molecular and mechanistic basis as to how phytochemicals and organochlorine compounds affect estrogen biosynthesis (i.e., aromatase function) in women. Research from Dr. Chen's and other laboratories have revealed that ER, aromatase, and ERRα are key players in breast cancer promotion and in cancer recurrence following endocrine treatment. Furthermore, proof-of-concept studies have revealed that these proteins are targets of endocrine disruptors. Based on these observations, we hypothesize that environmental chemicals will play critical roles in modulating breast cancer through ER, aromatase, and ERRα. The goal of this research is to develop screening assays for identifying and testing chemicals with relevance to known and suspected causes of estrogen-dependent breast cancer. Our collaborators include Richard Yip, Ph.D. (High Throughput Screening Core), Charles Wang, Ph.D. (Functional Genomics Core), Yate-Ching Yuan, Ph.D. (Bioinformatics Core), Christina Teng, Ph.D. (National Institute of Environmental Health Sciences), and Sandra Finestone, Psy.D. (Hope Wellness Center, Costa Mesa, CA).
 
 
Chemoprevention Research Program

Since the summer of 2004, Dr. Chen and 27 other investigators have initiated an effort to develop a chemoprevention research program at City of Hope. Through biweekly meetings, these Beckman researchers and clinicians exchange research information and ideas. Four research areas have recently been chosen to focus on. The immediate goal is to generate preliminary results in these new target areas that will lead to the development of multidiscipline translational chemoprevention research projects at our institution.

Our laboratory has found that grapes, mushrooms and pomegranate contain chemicals that can suppress aromatase activity. Therefore, a diet that includes grapes, mushrooms and pomegranate would be considered preventative against breast cancer. We are purifying and characterizing these natural anti-aromatase chemicals and evaluating their in vivo effects using animal experiments. The active chemicals in grapes have been found to be procyanidin dimers that are present at high concentrations in grape seeds. Melanie Palomares, M.D., (Population Sciences), Jeffrey Weitzel, M.D., (Clinical Cancer Genetics), Tim Synold, Pharm.D., (Experimental Therapeutics) and this laboratory have collaborated and initiated a grape seed extract clinical trial and a mushroom clinical trial based on the chemoprevention studies against breast cancer performed in our laboratory.

Furthermore, we have found that mushrooms contain chemicals that act as inhibitors of steroid 5-alpha reductase. Androgen plays a critical role in prostate cancer development. In the prostate, testosterone (an androgen) is converted to dihydrotestosterone (DHT), an androgen that is even more potent than testosterone. This conversion is catalyzed by the enzyme steroid 5-alpha reductase. An elevation of the steroid 5-alpha reductase activity in the prostate may cause benign prostate hyperplasia (a common problem in older men) and also promote the growth of prostate cancer. Animal experiments have been performed to evaluate the use of these phytochemicals as drugs in the prevention and/or treatment of prostate cancer. One clinical trial designed, based Dr. Chen's findings, is being carried out at City of Hope with Przemyslaw Twardowski, M.D. (Medical Oncology). A recent study in the Chen laboratory has revealed that the intake of mushrooms may reduce the incidence of metabolic diseases such as fatty liver and insulin resistance.

In addition, experiments have been carried out to show that blueberry contains phytochemicals that can suppress the proliferation and migration of triple negative breast cancer in cell culture and animals. Efforts are being made to initiate a blueberry clinical trial at City of Hope.
 
For more information on Dr. Chen, please click here.

Lab Members

Shiuan Chen, Ph.D. Lab Members

Hei (Jason) Chan, B.S.
Graduate Student
626-256-HOPE (4673), Ext. 63056
 
Zhike Chen, Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 6506
 
Masaya Kai, Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 60562
 
Noriko Kanaya, Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 65062
 
Karineh Petrossian, M.S.
Graduate Student
626-256-HOPE (4673), Ext. 65062
 
Yuan-Zhong Wang, Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 6305
 
Cynthie Wong , Ph.D.
Post-doctoral Fellow
626-256-HOPE (4673), Ext. 63056
 
Dujin Zhou, Ph.D.
Associate Research Scientist
626-256-HOPE (4673), Ext. 64908
 
Our Scientists

Our research laboratories are led by the best and brightest minds in scientific research.
 

Beckman Research Institute of City of Hope is internationally  recognized for its innovative biomedical research.
City of Hope is one of only 41 Comprehensive Cancer Centers in the country, the highest designation awarded by the National Cancer Institute to institutions that lead the way in cancer research, treatment, prevention and professional education.
Learn more about City of Hope's institutional distinctions, breakthrough innovations and collaborations.
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