Nature Genetics, ISSN 1061-4036, 08/2016, Volume 48, Issue 8, pp. 848 - 855
Recent studies have detailed the genomic landscape of primary endometrial cancers, but the evolution of these cancers into metastases has not been...
BREAST-CANCER | THERAPY | INSTABILITY | ADENOCARCINOMA | PANCREATIC-CANCER | GENETICS & HEREDITY | MUTATIONS | HYPERPLASIA | ARID1A | ESTROGEN-RECEPTOR | REVEALS | Abdominal Neoplasms - secondary | Genomics | Humans | Pelvic Neoplasms - genetics | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Phylogeny | Mutation - genetics | Disease Progression | Pelvic Neoplasms - secondary | Exome - genetics | Endometrial Neoplasms - genetics | Abdominal Neoplasms - genetics | Endometrial Neoplasms - pathology | Female | Biomarkers, Tumor - genetics | High-Throughput Nucleotide Sequencing | Evolution, Molecular | Complications and side effects | Genome-wide association studies | Endometrial cancer | Gene mutations | Genetic aspects | Metastasis | Health aspects | Risk factors | Methods | Studies | Biomedical research | Biopsy | Software | Mutation | Patients | Tumors | Precursor | Cancer genomics | Cancer evolution | Cancer
BREAST-CANCER | THERAPY | INSTABILITY | ADENOCARCINOMA | PANCREATIC-CANCER | GENETICS & HEREDITY | MUTATIONS | HYPERPLASIA | ARID1A | ESTROGEN-RECEPTOR | REVEALS | Abdominal Neoplasms - secondary | Genomics | Humans | Pelvic Neoplasms - genetics | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Phylogeny | Mutation - genetics | Disease Progression | Pelvic Neoplasms - secondary | Exome - genetics | Endometrial Neoplasms - genetics | Abdominal Neoplasms - genetics | Endometrial Neoplasms - pathology | Female | Biomarkers, Tumor - genetics | High-Throughput Nucleotide Sequencing | Evolution, Molecular | Complications and side effects | Genome-wide association studies | Endometrial cancer | Gene mutations | Genetic aspects | Metastasis | Health aspects | Risk factors | Methods | Studies | Biomedical research | Biopsy | Software | Mutation | Patients | Tumors | Precursor | Cancer genomics | Cancer evolution | Cancer
Journal Article
Oncogene, ISSN 0950-9232, 01/2009, Volume 28, Issue 1, pp. 31 - 40
Endometrioid adenocarcinoma is the most frequent form of endometrial cancer, usually developing in pre- and perimenopausal women. beta-catenin abnormalities...
β-catenin | Uterus | Hyperplasia | Estrogen | beta-catenin | estrogen | ENDOMETRIAL CARCINOMAS | CYCLIN D1 | MICROSATELLITE INSTABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | LEUKEMIA INHIBITORY FACTOR | E-CADHERIN | CELL BIOLOGY | NUCLEAR-LOCALIZATION | uterus | ONCOLOGY | GENETICS & HEREDITY | hyperplasia | MOUSE UTERUS | TRANSCRIPTIONAL TARGET | FEMALE REPRODUCTIVE-TRACT | COLON-CARCINOMA | Cell Proliferation | Endometrium - growth & development | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Infertility, Female - genetics | beta Catenin - genetics | Cell Differentiation - genetics | Animals | Cell Transformation, Neoplastic - genetics | Mice, Mutant Strains | Female | Mice | beta Catenin - physiology | Cell Transformation, Neoplastic - pathology | Endometrium - pathology | Disease Models, Animal
β-catenin | Uterus | Hyperplasia | Estrogen | beta-catenin | estrogen | ENDOMETRIAL CARCINOMAS | CYCLIN D1 | MICROSATELLITE INSTABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | LEUKEMIA INHIBITORY FACTOR | E-CADHERIN | CELL BIOLOGY | NUCLEAR-LOCALIZATION | uterus | ONCOLOGY | GENETICS & HEREDITY | hyperplasia | MOUSE UTERUS | TRANSCRIPTIONAL TARGET | FEMALE REPRODUCTIVE-TRACT | COLON-CARCINOMA | Cell Proliferation | Endometrium - growth & development | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Infertility, Female - genetics | beta Catenin - genetics | Cell Differentiation - genetics | Animals | Cell Transformation, Neoplastic - genetics | Mice, Mutant Strains | Female | Mice | beta Catenin - physiology | Cell Transformation, Neoplastic - pathology | Endometrium - pathology | Disease Models, Animal
Journal Article
Human Pathology, ISSN 0046-8177, 09/2017, Volume 67, pp. 69 - 77
Endometrial intraepithelial neoplasia (EIN) and atypical endometrial hyperplasia (AH) are histomorphologically defined precursors to endometrioid...
Clonal evolution | Endometrial hyperplasia | Endometrial intraepithelial neoplasia | Endometrioid adenocarcinoma | Next generation sequencing | PTEN | EIN | PATHOLOGY | CANCER | GENES | MUTATIONS | CARCINOMA | EXPRESSION | Immunohistochemistry | Microsatellite Instability | Cell Proliferation | Endometrial Hyperplasia - enzymology | Humans | Middle Aged | Endometrial Hyperplasia - pathology | DNA Copy Number Variations | Carcinoma in Situ - genetics | Carcinoma, Endometrioid - surgery | Carcinoma in Situ - enzymology | Carcinoma in Situ - surgery | Endometrial Neoplasms - genetics | DNA Mismatch Repair | Endometrial Hyperplasia - surgery | Aged, 80 and over | Female | Carcinoma, Endometrioid - genetics | Genetic Predisposition to Disease | Endometrial Neoplasms - enzymology | Carcinoma, Endometrioid - enzymology | Biomarkers, Tumor - analysis | Carcinoma in Situ - pathology | Endometrial Hyperplasia - genetics | Gene Dosage | Hysterectomy | DNA Repair Enzymes - analysis | Disease Progression | Phenotype | Biopsy | Endometrial Neoplasms - surgery | Endometrial Neoplasms - pathology | Aged | Biomarkers, Tumor - genetics | High-Throughput Nucleotide Sequencing | Mutation | Carcinoma, Endometrioid - pathology | Clonal Evolution | Adenocarcinoma | Gene mutations | Analysis | Hyperplasia | Genomics | Genetic research | Medical colleges | Proteins | Genes | Gynecology | Genomes | Deoxyribonucleic acid--DNA | Cancer | Esophagus
Clonal evolution | Endometrial hyperplasia | Endometrial intraepithelial neoplasia | Endometrioid adenocarcinoma | Next generation sequencing | PTEN | EIN | PATHOLOGY | CANCER | GENES | MUTATIONS | CARCINOMA | EXPRESSION | Immunohistochemistry | Microsatellite Instability | Cell Proliferation | Endometrial Hyperplasia - enzymology | Humans | Middle Aged | Endometrial Hyperplasia - pathology | DNA Copy Number Variations | Carcinoma in Situ - genetics | Carcinoma, Endometrioid - surgery | Carcinoma in Situ - enzymology | Carcinoma in Situ - surgery | Endometrial Neoplasms - genetics | DNA Mismatch Repair | Endometrial Hyperplasia - surgery | Aged, 80 and over | Female | Carcinoma, Endometrioid - genetics | Genetic Predisposition to Disease | Endometrial Neoplasms - enzymology | Carcinoma, Endometrioid - enzymology | Biomarkers, Tumor - analysis | Carcinoma in Situ - pathology | Endometrial Hyperplasia - genetics | Gene Dosage | Hysterectomy | DNA Repair Enzymes - analysis | Disease Progression | Phenotype | Biopsy | Endometrial Neoplasms - surgery | Endometrial Neoplasms - pathology | Aged | Biomarkers, Tumor - genetics | High-Throughput Nucleotide Sequencing | Mutation | Carcinoma, Endometrioid - pathology | Clonal Evolution | Adenocarcinoma | Gene mutations | Analysis | Hyperplasia | Genomics | Genetic research | Medical colleges | Proteins | Genes | Gynecology | Genomes | Deoxyribonucleic acid--DNA | Cancer | Esophagus
Journal Article
Carcinogenesis, ISSN 0143-3334, 2017, Volume 38, Issue 3, pp. 329 - 335
Endometrial carcinomas are histologically classified as endometrioid, assumed to originate from hyperplastic endometrium, or non-endometrioid carcinomas,...
AMPLIFICATION | PIK3CA | ONCOLOGY | BRAF MUTATIONS | CLASSIFICATION | ATYPICAL HYPERPLASIA | KRAS | CARCINOMA | CANCER | INTRAEPITHELIAL-NEOPLASIA | PTEN EXPRESSION | Receptor, Epidermal Growth Factor - genetics | Endometrial Hyperplasia - enzymology | Proto-Oncogene Proteins p21(ras) - genetics | Humans | Uterine Diseases - pathology | Endometrial Hyperplasia - pathology | Proto-Oncogene Proteins c-akt - genetics | Endometrial Neoplasms - genetics | Female | Precancerous Conditions - pathology | Carcinoma, Endometrioid - genetics | Precancerous Conditions - enzymology | Endometrial Neoplasms - enzymology | Carcinoma, Endometrioid - enzymology | Carcinogenesis - genetics | Endometrial Hyperplasia - genetics | Precancerous Conditions - genetics | Carcinogenesis - pathology | Phosphatidylinositol 3-Kinases - genetics | Class I Phosphatidylinositol 3-Kinases | Uterine Diseases - enzymology | Uterine Diseases - genetics | Endometrial Neoplasms - pathology | DNA, Neoplasm - genetics | Mutation | Carcinoma, Endometrioid - pathology
AMPLIFICATION | PIK3CA | ONCOLOGY | BRAF MUTATIONS | CLASSIFICATION | ATYPICAL HYPERPLASIA | KRAS | CARCINOMA | CANCER | INTRAEPITHELIAL-NEOPLASIA | PTEN EXPRESSION | Receptor, Epidermal Growth Factor - genetics | Endometrial Hyperplasia - enzymology | Proto-Oncogene Proteins p21(ras) - genetics | Humans | Uterine Diseases - pathology | Endometrial Hyperplasia - pathology | Proto-Oncogene Proteins c-akt - genetics | Endometrial Neoplasms - genetics | Female | Precancerous Conditions - pathology | Carcinoma, Endometrioid - genetics | Precancerous Conditions - enzymology | Endometrial Neoplasms - enzymology | Carcinoma, Endometrioid - enzymology | Carcinogenesis - genetics | Endometrial Hyperplasia - genetics | Precancerous Conditions - genetics | Carcinogenesis - pathology | Phosphatidylinositol 3-Kinases - genetics | Class I Phosphatidylinositol 3-Kinases | Uterine Diseases - enzymology | Uterine Diseases - genetics | Endometrial Neoplasms - pathology | DNA, Neoplasm - genetics | Mutation | Carcinoma, Endometrioid - pathology
Journal Article
Gynecologic Oncology, ISSN 0090-8258, 2014, Volume 135, Issue 3, pp. 552 - 559
Abstract Objective Women with atypical hyperplasia (AH) are often found to have endometrial carcinoma (EC) at hysterectomy. The purpose of this study was to...
Hematology, Oncology and Palliative Medicine | Obstetrics and Gynecology | Epigenetics | Methylation | Endometrial carcinoma | Endometrium | Atypical hyperplasia | BLADDER-CANCER | DIAGNOSIS | CELLS | PROMOTER METHYLATION | ADENOCARCINOMA | MARKERS | CERVICAL-CANCER | IDENTIFICATION | OBSTETRICS & GYNECOLOGY | ONCOLOGY | GENES | EXPRESSION | DNA Methylation | Epigenomics | Endometrial Neoplasms - genetics | Humans | Endometrial Hyperplasia - genetics | Endometrial Neoplasms - pathology | Female | Male | Biomarkers, Tumor - genetics | Endometrial Hyperplasia - pathology | Carcinoma | Hyperplasia | DNA | Genetic research | Genetic aspects | Cancer
Hematology, Oncology and Palliative Medicine | Obstetrics and Gynecology | Epigenetics | Methylation | Endometrial carcinoma | Endometrium | Atypical hyperplasia | BLADDER-CANCER | DIAGNOSIS | CELLS | PROMOTER METHYLATION | ADENOCARCINOMA | MARKERS | CERVICAL-CANCER | IDENTIFICATION | OBSTETRICS & GYNECOLOGY | ONCOLOGY | GENES | EXPRESSION | DNA Methylation | Epigenomics | Endometrial Neoplasms - genetics | Humans | Endometrial Hyperplasia - genetics | Endometrial Neoplasms - pathology | Female | Male | Biomarkers, Tumor - genetics | Endometrial Hyperplasia - pathology | Carcinoma | Hyperplasia | DNA | Genetic research | Genetic aspects | Cancer
Journal Article
Modern Pathology, ISSN 0893-3952, 03/2013, Volume 26, Issue 3, pp. 428 - 434
ARID1A (AT-rich interactive domain 1A) has recently been identified as a tumor suppressor gene in various, predominantly gynecological cancers. We wanted to...
ARID1A | carcinoma | endometrial | REMODELING GENE ARID1A | PROTEIN EXPRESSION | TISSUE MICROARRAYS | TUMOR-SUPPRESSOR | MUTATIONS | PATHOLOGY | CLEAR-CELL CARCINOMA | CANCER | PROGRESSION | Immunohistochemistry | Nuclear Proteins - analysis | Prognosis | Prospective Studies | Oligonucleotide Array Sequence Analysis | Endometrial Neoplasms - mortality | Tissue Array Analysis | Endometrial Hyperplasia - mortality | Humans | Middle Aged | RNA, Messenger - analysis | Endometrial Hyperplasia - pathology | Carcinoma, Endometrioid - therapy | Carcinoma, Endometrioid - chemistry | Endometrial Hyperplasia - metabolism | Neoplasm Grading | Endometrial Neoplasms - genetics | Time Factors | Female | Retrospective Studies | Endometrial Hyperplasia - therapy | Nuclear Proteins - genetics | Carcinoma, Endometrioid - genetics | Carcinoma, Endometrioid - secondary | Endometrial Neoplasms - chemistry | Biomarkers, Tumor - analysis | Neoplasm Invasiveness | Down-Regulation | Kaplan-Meier Estimate | Endometrial Hyperplasia - genetics | Transcription Factors - genetics | Chi-Square Distribution | Carcinoma, Endometrioid - mortality | Endometrial Neoplasms - therapy | Endometrial Neoplasms - pathology | Aged | Biomarkers, Tumor - genetics | Transcription Factors - analysis | Index Medicus
ARID1A | carcinoma | endometrial | REMODELING GENE ARID1A | PROTEIN EXPRESSION | TISSUE MICROARRAYS | TUMOR-SUPPRESSOR | MUTATIONS | PATHOLOGY | CLEAR-CELL CARCINOMA | CANCER | PROGRESSION | Immunohistochemistry | Nuclear Proteins - analysis | Prognosis | Prospective Studies | Oligonucleotide Array Sequence Analysis | Endometrial Neoplasms - mortality | Tissue Array Analysis | Endometrial Hyperplasia - mortality | Humans | Middle Aged | RNA, Messenger - analysis | Endometrial Hyperplasia - pathology | Carcinoma, Endometrioid - therapy | Carcinoma, Endometrioid - chemistry | Endometrial Hyperplasia - metabolism | Neoplasm Grading | Endometrial Neoplasms - genetics | Time Factors | Female | Retrospective Studies | Endometrial Hyperplasia - therapy | Nuclear Proteins - genetics | Carcinoma, Endometrioid - genetics | Carcinoma, Endometrioid - secondary | Endometrial Neoplasms - chemistry | Biomarkers, Tumor - analysis | Neoplasm Invasiveness | Down-Regulation | Kaplan-Meier Estimate | Endometrial Hyperplasia - genetics | Transcription Factors - genetics | Chi-Square Distribution | Carcinoma, Endometrioid - mortality | Endometrial Neoplasms - therapy | Endometrial Neoplasms - pathology | Aged | Biomarkers, Tumor - genetics | Transcription Factors - analysis | Index Medicus
Journal Article
Modern Pathology, ISSN 0893-3952, 11/2012, Volume 25, Issue 11, pp. 1508 - 1515
We investigated the relationship between frequently deregulated microRNAs (miRNAs) and enodometrial pathology in an attempt to find the most dependable miRNA...
PTEN | endometrial hyperplasia and carcinoma | microRNA | OVARIAN-CANCER | PATHOLOGY | SIGNATURE | PROFILE | MICRORNA EXPRESSION | CARCINOMA | BIOPSIES | PROGRESSION | CLINICOPATHOLOGICAL FEATURES | EPIGENETIC ALTERATIONS | IMMUNOHISTOCHEMISTRY | Immunohistochemistry | Predictive Value of Tests | Adenocarcinoma - pathology | Endometrium - enzymology | Endometrial Hyperplasia - enzymology | Humans | Middle Aged | PTEN Phosphohydrolase - analysis | Endometrial Hyperplasia - pathology | Formaldehyde | Paraffin Embedding | Endometrial Neoplasms - genetics | Fixatives | Cell Transformation, Neoplastic - genetics | MicroRNAs - analysis | Sensitivity and Specificity | Adult | Female | Precancerous Conditions - pathology | Adenocarcinoma - genetics | Tissue Fixation | Real-Time Polymerase Chain Reaction | Precancerous Conditions - enzymology | Endometrial Neoplasms - enzymology | Biomarkers, Tumor - analysis | Adenocarcinoma - enzymology | Endometrial Hyperplasia - genetics | Gene Expression Profiling - methods | Chi-Square Distribution | Reverse Transcriptase Polymerase Chain Reaction | Cell Transformation, Neoplastic - metabolism | Precancerous Conditions - genetics | Disease Progression | Endometrial Neoplasms - pathology | Aged | Cell Transformation, Neoplastic - pathology | Endometrium - pathology
PTEN | endometrial hyperplasia and carcinoma | microRNA | OVARIAN-CANCER | PATHOLOGY | SIGNATURE | PROFILE | MICRORNA EXPRESSION | CARCINOMA | BIOPSIES | PROGRESSION | CLINICOPATHOLOGICAL FEATURES | EPIGENETIC ALTERATIONS | IMMUNOHISTOCHEMISTRY | Immunohistochemistry | Predictive Value of Tests | Adenocarcinoma - pathology | Endometrium - enzymology | Endometrial Hyperplasia - enzymology | Humans | Middle Aged | PTEN Phosphohydrolase - analysis | Endometrial Hyperplasia - pathology | Formaldehyde | Paraffin Embedding | Endometrial Neoplasms - genetics | Fixatives | Cell Transformation, Neoplastic - genetics | MicroRNAs - analysis | Sensitivity and Specificity | Adult | Female | Precancerous Conditions - pathology | Adenocarcinoma - genetics | Tissue Fixation | Real-Time Polymerase Chain Reaction | Precancerous Conditions - enzymology | Endometrial Neoplasms - enzymology | Biomarkers, Tumor - analysis | Adenocarcinoma - enzymology | Endometrial Hyperplasia - genetics | Gene Expression Profiling - methods | Chi-Square Distribution | Reverse Transcriptase Polymerase Chain Reaction | Cell Transformation, Neoplastic - metabolism | Precancerous Conditions - genetics | Disease Progression | Endometrial Neoplasms - pathology | Aged | Cell Transformation, Neoplastic - pathology | Endometrium - pathology
Journal Article
Human Pathology, ISSN 0046-8177, 06/2001, Volume 32, Issue 6, pp. 569 - 577
Four different genetic abnormalities may occur in endometrioid adenocarcinomas of the endometrium (mircosatellite instability and mutations in the , and...
microsatellite instability | β-catenin | MLH-1 methylation | PTEN, k-RAS | Endometrial carcinoma | molecular pathology | PTEN | Molecular pathology | k-RAS | Microsatellite instability | beta-catenin | BETA-CATENIN GENE | PROMOTER HYPERMETHYLATION | endometrial carcinoma | GENETICALLY UNSTABLE CANCERS | PATHOLOGY | ISLAND METHYLATOR PHENOTYPE | COLORECTAL-CANCER | SEROUS CARCINOMA | SOMATIC FRAMESHIFT MUTATIONS | REPLICATION ERRORS | KI-RAS ONCOGENE | Phosphoric Monoester Hydrolases - genetics | beta Catenin | Cytoskeletal Proteins - genetics | Humans | Trans-Activators | Endometrial Hyperplasia - genetics | Genes, p53 - genetics | Microsatellite Repeats - genetics | DNA Methylation | Endometrial Neoplasms - genetics | PTEN Phosphohydrolase | Female | Mutation | Tumor Suppressor Proteins | Genes, ras - genetics | Carcinoma | Colon cancer | Hyperplasia | Development and progression | Bone morphogenetic proteins | Tumor proteins | Transforming growth factors | Methylation | Chromosomes | Cancer
microsatellite instability | β-catenin | MLH-1 methylation | PTEN, k-RAS | Endometrial carcinoma | molecular pathology | PTEN | Molecular pathology | k-RAS | Microsatellite instability | beta-catenin | BETA-CATENIN GENE | PROMOTER HYPERMETHYLATION | endometrial carcinoma | GENETICALLY UNSTABLE CANCERS | PATHOLOGY | ISLAND METHYLATOR PHENOTYPE | COLORECTAL-CANCER | SEROUS CARCINOMA | SOMATIC FRAMESHIFT MUTATIONS | REPLICATION ERRORS | KI-RAS ONCOGENE | Phosphoric Monoester Hydrolases - genetics | beta Catenin | Cytoskeletal Proteins - genetics | Humans | Trans-Activators | Endometrial Hyperplasia - genetics | Genes, p53 - genetics | Microsatellite Repeats - genetics | DNA Methylation | Endometrial Neoplasms - genetics | PTEN Phosphohydrolase | Female | Mutation | Tumor Suppressor Proteins | Genes, ras - genetics | Carcinoma | Colon cancer | Hyperplasia | Development and progression | Bone morphogenetic proteins | Tumor proteins | Transforming growth factors | Methylation | Chromosomes | Cancer
Journal Article
Differentiation, ISSN 0301-4681, 10/2016, Volume 92, Issue 4, pp. 204 - 215
SOX9 is a high mobility group transcription factor that is required in many biological processes, including cartilage differentiation, endoderm progenitor...
Transgenic mouse | Sox9 | Uterus | Endometrium | Cancer | CELLS | DEVELOPMENTAL BIOLOGY | TUMORIGENICITY | POLYPS | CELL BIOLOGY | IN-VIVO | MUTATIONS | DIFFERENTIATION | UP-REGULATION | CARCINOMA | Uterine Neoplasms - genetics | Uterus - pathology | Epithelium - pathology | Epithelium - growth & development | Uterine Neoplasms - pathology | Humans | Uterus - metabolism | Endometrium - growth & development | Gene Expression Regulation, Neoplastic | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Receptors, Progesterone - genetics | Animals | Female | Mice | Endometrium - pathology | SOX9 Transcription Factor - genetics | endometrium | cancer | uterus | transgenic mouse
Transgenic mouse | Sox9 | Uterus | Endometrium | Cancer | CELLS | DEVELOPMENTAL BIOLOGY | TUMORIGENICITY | POLYPS | CELL BIOLOGY | IN-VIVO | MUTATIONS | DIFFERENTIATION | UP-REGULATION | CARCINOMA | Uterine Neoplasms - genetics | Uterus - pathology | Epithelium - pathology | Epithelium - growth & development | Uterine Neoplasms - pathology | Humans | Uterus - metabolism | Endometrium - growth & development | Gene Expression Regulation, Neoplastic | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Receptors, Progesterone - genetics | Animals | Female | Mice | Endometrium - pathology | SOX9 Transcription Factor - genetics | endometrium | cancer | uterus | transgenic mouse
Journal Article
BJOG: An International Journal of Obstetrics & Gynaecology, ISSN 1470-0328, 09/2017, Volume 124, Issue 10, pp. 1576 - 1583
Objective To report the response to progestin therapy in young women with endometrial complex atypical hyperplasia (CAH) or FIGO grade 1 endometrial...
endometrial cancer | mismatch repair | Complex atypical hyperplasia | Lynch syndrome | PROGNOSTIC-FACTORS | PREMENOPAUSAL WOMEN | FAMILY-HISTORY | CANCER | OBSTETRICS & GYNECOLOGY | REPRODUCTIVE OUTCOMES | THERAPY | FERTILITY-SPARING MANAGEMENT | ORAL PROGESTIN | CARCINOMA | Immunohistochemistry | Adenocarcinoma - pathology | Progestins - therapeutic use | Humans | Middle Aged | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Adenocarcinoma - drug therapy | Endometrial Hyperplasia - drug therapy | Endometrial Neoplasms - genetics | DNA Mismatch Repair | Adult | Endometrial Neoplasms - drug therapy | Endometrial Neoplasms - pathology | Female | Adenocarcinoma - genetics | Adenocarcinoma | Proteins | Medical research | Endometrial cancer | Hyperplasia | Young women | Medicine, Experimental | Invasiveness | Gynecology | Malignancy | DNA repair | Body mass index | MMR protein | Body mass | Progestin | Medical prognosis | Mismatch repair | Biomarkers | Protein expression | Hormone replacement therapy | Health risk assessment | Age | Endometrium
endometrial cancer | mismatch repair | Complex atypical hyperplasia | Lynch syndrome | PROGNOSTIC-FACTORS | PREMENOPAUSAL WOMEN | FAMILY-HISTORY | CANCER | OBSTETRICS & GYNECOLOGY | REPRODUCTIVE OUTCOMES | THERAPY | FERTILITY-SPARING MANAGEMENT | ORAL PROGESTIN | CARCINOMA | Immunohistochemistry | Adenocarcinoma - pathology | Progestins - therapeutic use | Humans | Middle Aged | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Adenocarcinoma - drug therapy | Endometrial Hyperplasia - drug therapy | Endometrial Neoplasms - genetics | DNA Mismatch Repair | Adult | Endometrial Neoplasms - drug therapy | Endometrial Neoplasms - pathology | Female | Adenocarcinoma - genetics | Adenocarcinoma | Proteins | Medical research | Endometrial cancer | Hyperplasia | Young women | Medicine, Experimental | Invasiveness | Gynecology | Malignancy | DNA repair | Body mass index | MMR protein | Body mass | Progestin | Medical prognosis | Mismatch repair | Biomarkers | Protein expression | Hormone replacement therapy | Health risk assessment | Age | Endometrium
Journal Article
Molecular Human Reproduction, ISSN 1360-9947, 2014, Volume 20, Issue 8, pp. 776 - 786
In the uterus, epithelial cell proliferation changes during the estrous cycle and pregnancy. Uncontrolled epithelial cell proliferation results in implantation...
Endometrial hyperplasia | Proliferation | Uterus | epithelial cell | Transforming growth factor β | TGF-BETA | proliferation | PROGESTERONE | transforming growth factor beta | DEVELOPMENTAL BIOLOGY | PREGNANCY | OBSTETRICS & GYNECOLOGY | GROWTH-FACTOR-BETA | REPRODUCTIVE BIOLOGY | uterus | endometrial hyperplasia | SUPERFAMILY | PROTEINS | EXPRESSION | FOXA2 | FGF10 | Cell Proliferation - genetics | Receptors, Transforming Growth Factor beta - genetics | Epithelial Cells - metabolism | Transforming Growth Factor beta1 - metabolism | Uterus - metabolism | Cell Proliferation - physiology | Cells, Cultured | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Transforming Growth Factor beta1 - genetics | Receptors, Peptide - genetics | Mice, Knockout | Animals | Endometrial Hyperplasia - metabolism | Receptors, Transforming Growth Factor beta - metabolism | Uterus - cytology | Female | Mice | Epithelial Cells - cytology | Receptors, Peptide - metabolism | transforming growth factor β
Endometrial hyperplasia | Proliferation | Uterus | epithelial cell | Transforming growth factor β | TGF-BETA | proliferation | PROGESTERONE | transforming growth factor beta | DEVELOPMENTAL BIOLOGY | PREGNANCY | OBSTETRICS & GYNECOLOGY | GROWTH-FACTOR-BETA | REPRODUCTIVE BIOLOGY | uterus | endometrial hyperplasia | SUPERFAMILY | PROTEINS | EXPRESSION | FOXA2 | FGF10 | Cell Proliferation - genetics | Receptors, Transforming Growth Factor beta - genetics | Epithelial Cells - metabolism | Transforming Growth Factor beta1 - metabolism | Uterus - metabolism | Cell Proliferation - physiology | Cells, Cultured | Endometrial Hyperplasia - genetics | Endometrial Hyperplasia - pathology | Transforming Growth Factor beta1 - genetics | Receptors, Peptide - genetics | Mice, Knockout | Animals | Endometrial Hyperplasia - metabolism | Receptors, Transforming Growth Factor beta - metabolism | Uterus - cytology | Female | Mice | Epithelial Cells - cytology | Receptors, Peptide - metabolism | transforming growth factor β
Journal Article