Chin‐Yo Lin
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View article: Targeting Liver X Receptors in Cancer Drug Discovery
Targeting Liver X Receptors in Cancer Drug Discovery Open
Liver X receptors (LXRs) are members of the nuclear receptor superfamily of ligand-dependent transcription factors. LXRα is predominantly expressed in metabolic tissues, whereas LXRβ is ubiquitously expressed. Upon ligand binding, they reg…
View article: Liver X Receptor Ligand GAC0001E5 Downregulates Antioxidant Capacity and ERBB2/HER2 Expression in HER2-Positive Breast Cancer Cells
Liver X Receptor Ligand GAC0001E5 Downregulates Antioxidant Capacity and ERBB2/HER2 Expression in HER2-Positive Breast Cancer Cells Open
The HER2-positive subtype accounts for approximately one-fifth of all breast cancers. Insensitivity and development of acquired resistance to targeted therapies in some patients contribute to their poor prognosis. HER2 overexpression is as…
View article: Figure S2 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Figure S2 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
IHC results for p16 and Mcm7.
View article: Figure S1 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Figure S1 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
H&E images of cancer and epithelium.
View article: Figure S2 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Figure S2 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
IHC results for p16 and Mcm7.
View article: Table S2 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Table S2 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
IHC conditions and information for antibodies and chemicals.
View article: Figure S3 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Figure S3 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
Cancer size data from E6/E7 mice.
View article: Table S1 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Table S1 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
Description of mouse strains.
View article: Table S1 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Table S1 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
Description of mouse strains.
View article: Table S2 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Table S2 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
IHC conditions and information for antibodies and chemicals.
View article: Supplementary Information from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Supplementary Information from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
Supplemental materials and methods, supplemental figure legends
View article: Figure S3 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Figure S3 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
Cancer size data from E6/E7 mice.
View article: Data from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Data from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
Tumor-suppressor genes (TSG) are often deleted or transcriptionally suppressed in cancer. PGR codes for progesterone receptor (PR), a transcription factor whose function depends on its ligand. Although PR expression is often undetectable i…
View article: Data from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Data from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
Tumor-suppressor genes (TSG) are often deleted or transcriptionally suppressed in cancer. PGR codes for progesterone receptor (PR), a transcription factor whose function depends on its ligand. Although PR expression is often undetectable i…
View article: Figure S1 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Figure S1 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
H&E images of cancer and epithelium.
View article: Figure S4 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Figure S4 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
ESR1 expression levels and CNV data.
View article: Figure S4 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Figure S4 from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
ESR1 expression levels and CNV data.
View article: Supplementary Information from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer
Supplementary Information from Progesterone Receptor Is a Haploinsufficient Tumor-Suppressor Gene in Cervical Cancer Open
Supplemental materials and methods, supplemental figure legends
View article: Supplementary Tables 1-3 from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome
Supplementary Tables 1-3 from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome Open
Supplementary Tables 1-3 from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome
View article: Data from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome
Data from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome Open
The beneficial effect of the selective estrogen receptor (ER) modulator tamoxifen in the treatment and prevention of breast cancer is assumed to be through its ability to antagonize the stimulatory actions of estrogen, although tamoxifen c…
View article: Supplementary Table 1 from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer
Supplementary Table 1 from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer Open
Supplementary Table 1 from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer
View article: Data from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome
Data from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome Open
The beneficial effect of the selective estrogen receptor (ER) modulator tamoxifen in the treatment and prevention of breast cancer is assumed to be through its ability to antagonize the stimulatory actions of estrogen, although tamoxifen c…
View article: Data from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer
Data from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer Open
Estrogen receptors (ER) and nuclear factor-κB (NF-κB) are known to play important roles in breast cancer, but these factors are generally thought to repress each other's activity. However, we have recently found that ER and NF-κB can also …
View article: Data from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer
Data from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer Open
Estrogen receptors (ER) and nuclear factor-κB (NF-κB) are known to play important roles in breast cancer, but these factors are generally thought to repress each other's activity. However, we have recently found that ER and NF-κB can also …
View article: Supplementary Tables 1-3 from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome
Supplementary Tables 1-3 from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome Open
Supplementary Tables 1-3 from Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells and Correlations with Clinical Outcome
View article: Supplementary Table 1 from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer
Supplementary Table 1 from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer Open
Supplementary Table 1 from Positive Cross-Talk between Estrogen Receptor and NF-κB in Breast Cancer
View article: Liver X Receptor Inverse Agonist GAC0001E5 Impedes Glutaminolysis and Disrupts Redox Homeostasis in Breast Cancer Cells
Liver X Receptor Inverse Agonist GAC0001E5 Impedes Glutaminolysis and Disrupts Redox Homeostasis in Breast Cancer Cells Open
Liver X receptors (LXRs) are members of the nuclear receptor family of ligand-dependent transcription factors which regulate the expression of lipid and cholesterol metabolism genes. Moreover, LXRs and their ligands have been shown to inhi…
View article: A Novel Liver X Receptor Inverse Agonist Impairs Cholesterol and Phospholipid Metabolism and Induces Apoptosis and Necroptosis in Pancreatic Ductal Adenocarcinoma Cells
A Novel Liver X Receptor Inverse Agonist Impairs Cholesterol and Phospholipid Metabolism and Induces Apoptosis and Necroptosis in Pancreatic Ductal Adenocarcinoma Cells Open
Pancreatic ductal adenocarcinoma (PDAC) is an aggressive disease with a high mortality rate and few effective treatments. A growing area of cancer therapeutics seeks to exploit the metabolic dysregulation of cancer cells, such as glucose, …
View article: Non-Metabolic Functions of PKM2 Contribute to Cervical Cancer Cell Proliferation Induced by the HPV16 E7 Oncoprotein
Non-Metabolic Functions of PKM2 Contribute to Cervical Cancer Cell Proliferation Induced by the HPV16 E7 Oncoprotein Open
Pyruvate kinase M2 (PKM2) mainly catalyzes glycolysis, but it also exerts non-glycolytic functions in several cancers. While it has been shown to interact with the human papillomavirus 16 (HPV16) E7 oncoprotein, the functional significance…