Search results for "Hormone receptor"

showing 10 items of 85 documents

Targeted Therapies Overcoming Endocrine Resistance in Hormone Receptor-Positive Breast Cancer

2015

Breast cancer is a heterogeneous disease with different molecular subtypes. Most tumours are hormone receptor positive (luminal subtype) with potential endocrine responsiveness. Endocrine therapy is commonly used in these patients. Disease progression caused by endocrine resistance represents a significant challenge in the treatment of breast cancer. To understand the mechanisms of resistance of long-term oestrogen-deprived breast cancer cells, it is important to focus on cross-talk between steroid receptor signalling and other growth factor receptors and intracellular pathways. (Pre-)clinical trials showed that co-targeting these pathways can restore endocrine sensitivity. The focus of the…

Everolimusbusiness.industryReview ArticlePharmacologyPalbociclibmedicine.diseaseBreast cancerOncologyGrowth factor receptorHormone receptormedicineCancer researchEndocrine systemSurgerybusinessProtein kinase BPI3K/AKT/mTOR pathwaymedicine.drugBreast Care
researchProduct

A phase I/Ib study evaluating GDC-0077 (inavolisib) + palbociclib (palbo) + fulvestrant in patients (pts) with PIK3CA-mutant (mut), hormone receptor-…

2021

FulvestrantHormone receptorbusiness.industryMutantHER2 negativeCancer researchmedicineIn patientPalbociclibmedicine.diseasebusinessMetastatic breast cancermedicine.drugSenologie - Zeitschrift für Mammadiagnostik und -therapie
researchProduct

New point mutation (R243W) in the hormone binding domain of the c‐erbA β1 gene in a family with generalized resistance to thyroid hormone

1996

Two years after the first mutation on exon 7 in the carboxy-terminal part of the hinge domain (D) was reported (Behr and Loos 1992), we have identified the second mutation on exon 7 in patients with GRTH. Interestingly, our mutation it is not located in the two previously described "hot spot regions", but instead very close to the hinge domain (D) of the receptor protein that is essential for the function of the hormone binding domain (E) (Lin et al., 1991). Confirming the observation that the majority of single base substitutions causing human genetic diseases or DNA polymorphisms follow the hot spot mutation rule of CG to TG and CG to CA transition (Barker et al., 1984), an additional CpG…

Geneticsmedicine.medical_specialtyThyroid hormone receptorPoint mutationBiologyThyroid hormone receptor betaExonEndocrinologyCpG siteInternal medicinemedicineGeneticsReceptorGeneGenetics (clinical)Binding domainHuman Mutation
researchProduct

Isoflavonoid-based bone-sparing treatments exert a low activity on reproductive organs and on hepatic metabolism of estradiol in ovariectomized rats

2007

International audience; The use of soy isoflavones is a potential alternative to hormone replacement therapy in post-menopausal bone-loss prevention. Nevertheless, phytoestrogens can target other organs and may disrupt cell proliferation, or could modify endogenous steroid hormone metabolism. These mechanisms could be linked to an increased risk of developing cancer. We therefore studied the possible side effects of such treatments in an experimental model of menopause. Forty adult female Wistar rats were ovariectomized and fed with a genistein-, daidzein- or equol-supplemented diet at bone-sparing levels (10 mg/kg BW/day) for 3 months. The estrogenic effects were assessed by histological a…

GenisteinEstrogen receptorToxicologychemistry.chemical_compound0302 clinical medicineCytochrome P-450 Enzyme SystemBone Density[SDV.IDA]Life Sciences [q-bio]/Food engineeringESTROGEN RECEPTORS0303 health sciencesEstradiolfood and beveragesOrgan SizeEquolGenistein3. Good healthCYTOCHROME P450SOY ISOFLAVONEHormone receptor030220 oncology & carcinogenesisVaginaMicrosomes LiverFemaleMenopauseEQUOLmedicine.medical_specialtymedicine.drug_classOvariectomyPhytoestrogensBiology03 medical and health sciencesProliferating Cell Nuclear AntigenInternal medicinemedicineUTEROTROPHYAnimals[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringRats Wistar030304 developmental biologyPharmacologyUterusDaidzeinIsoflavonesRatsDisease Models AnimalEndocrinologyGene Expression RegulationchemistryEstrogenESTRADIOL METABOLISMOsteoporosisPhytoestrogensSteroid hormone metabolism
researchProduct

Zum Steroidhormonrezeptorenstatus kolorektaler Karzinome

1990

Zur Analyse des Steroidhormonrezeptorenstatus kolorektaler Karzinome wurde der Ostrogen- und Progesteronrezeptorgehalt von 26 aufeinanderfolgenden Tumoren bestimmt. In alien Proben lag die Estradiol-Rezeptorbindungskapazitat unterhalb des mestechnischen Cut-offs von 2 fmol/mg Cytosolprotein. In 4 von 26 Tumorproben (15%) waren Progesteron-Rezeptorspiegel zwischen 13 und 23 fmol/ mg Cytosolprotein nachweisbar. Aufgrund des Nachweises von Stero-idhormonrezeptoren in einigen Fallen und vereinzelter Berichte in der Literatur uber Remissionen unter Hormontherapie kolorektaler Karzinome scheinen weitere In-vitro- und In-vivo-Versuche angezeigt, die Hormonabhangigkeit des kolorektalen Karzinoms zu…

GynecologyCancer Researchmedicine.medical_specialtyOncologySteroid hormone receptorbusiness.industrymedicineHematologybusinessOncology Research and Treatment
researchProduct

A randomized, open-label, multicentre, phase IV study evaluating palbociclib plus endocrine treatment versus a chemotherapy based treatment strategy …

2017

TPS1115 Background: Although endocrine based therapy is recommended as first-line treatment in metastatic breast cancer (MBC) in patients with an HER2-/HR+ tumour up to 50% of the patients receive chemotherapy. Palbociclib (P) a CDK4/6 inhibitor improves PFS by 42% in endocrine sensitive and resistant HER2-/HR+ MBC when added to an endocrine therapy (ET). Patients included in clinical trials are often criticised not to be representative for real world breast cancer patients. Methods: Patients with first-line HER2-/HR+ MBC who are candidate for mono-chemotherapy will be eligible to be randomised 1:1 to receive either P plus ET per label or mono-chemotherapy per investigator´s choice with or…

GynecologyOncologyCancer Researchmedicine.medical_specialtyChemotherapybusiness.industrymedicine.medical_treatmentHER2 negativePalbociclibmedicine.diseaseMetastatic breast cancerOncologyHormone receptorInternal medicinemedicineEndocrine systemIn patientOpen labelbusinessJournal of Clinical Oncology
researchProduct

Estrogen levels in premenopausal (prem) patients (pts) with hormone-receptor positive (HR+) early breast cancer (BC) receiving adjuvant triptorelin (…

2014

585 Background: Optimal endocrine therapy for prem pts with early HR+ BC may depend on complete estrogen suppression with GnRH-A, and is crucial for those receiving concurrent aromatase inhibitors (AI). SOFT-EST is a prospective substudy of the phase III SOFT trial. Aims of SOFT-EST are to describe estradiol (E2), estrone (E1) and estrone sulphate (E1S) during monthly Trip + E or T and to assess if there is a group in E+Trip with suboptimal estrogen suppression (SES). Methods: All pts enrolled in SOFT from selected centers who consented, selected Trip as ovarian function suppression method and were randomized to E+Trip or T+Trip were enrolled in SOFT-EST until reaching the accrual goal (E=9…

GynecologyOncologyCancer Researchmedicine.medical_specialtybiologymedicine.drug_classbusiness.industryEstroneTriptorelinchemistry.chemical_compoundOncologyExemestanechemistryEstrogenHormone receptorInternal medicinebiology.proteinmedicineAromatasebusinesshuman activitiesTamoxifenmedicine.drugBlood samplingJournal of Clinical Oncology
researchProduct

Fulvestrant and trastuzumab in patients with luminal HER2-positive advanced breast cancer (ABC): an Italian real-world experience (HERMIONE 9)

2021

Purpose: The most appropriate therapy for HR + /HER2-positive (HER2 +) advanced breast cancer (ABC) is a matter of debate. Co-targeting of both receptors represents an attractive strategy to overcome the cross-talk between them. Methods: The HERMIONE 9 is an observational retrospective multicentric study which aimed to describe the clinical outcome of patients with HR + /HER2 + ABC who received the combination of Fulvestrant (F) and Trastuzumab (T) as part of their routine treatment at 10 Italian Institutions. Results: Eighty-seven patients were included. Median age was 63 (range, 35–87) years. The median number of previous treatments was 3 (range, 0–10) and F and T were administered as ≥ 3…

HER2 positiveOncologyCancer Researchmedicine.medical_specialtySettore MED/06 - Oncologia MedicaReceptor ErbB-2Advanced breastBreast NeoplasmsBreast cancerMaintenance therapyTrastuzumabInternal medicineAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansFulvestrantRetrospective StudiesHormone receptor positiveFulvestrantbusiness.industryCancerMiddle AgedTrastuzumabmedicine.diseaseItalyOncologyCohortAdvanced breast cancerFemalePertuzumabbusinessmedicine.drugBreast Cancer Research and Treatment
researchProduct

Employment of vasopressin receptor antagonists in management of hyponatraemia and volume overload in some clinical conditions

2015

Summary What is known and objective Hyponatraemia, the most common electrolyte imbalance occurring in hospitalized subjects, is usually classified as hypovolaemic, euvolaemic or hypervolaemic. Hyponatraemia is a predictor of death among subjects with chronic heart failure and cirrhosis. The inappropriate secretion of the antidiuretic hormone (AVP) seems to be of pivotal importance in the decline of serum sodium concentration in these clinical conditions. The objective of this review was to summarize recent progress in management of hyponatraemia in SIADH, cirrhosis and heart failure. Methods Literature searches were conducted on the topics of hyponatraemia and vasopressin receptor antagonis…

Heart FailureLiver CirrhosisPharmacologyAquapheresismedicine.medical_specialtyCirrhosisbusiness.industrymedicine.medical_treatmentSodiumVolume overloadmedicine.diseasePlaceboHypertonic salineInappropriate ADH SyndromeAnesthesiaHeart failuremedicineHumansPharmacology (medical)DecompensationbusinessIntensive care medicineAntidiuretic Hormone Receptor AntagonistsHyponatremiaAntidiureticJournal of Clinical Pharmacy and Therapeutics
researchProduct

Resistance to thyroid hormones. Study of an affected kindred diagnosed at neonatal age

1998

Resistance to thyroid hormones (RTH) is a rare condition of reduced activity of thyroid hormones on peripheral tissues and/or reduced suppression of TSH secretion by thyroid hormones. The disease is characterised by high serum levels of T3, T4, fT3 and fT4, and by unexpectedly normal or high TSH levels. The origin of the resistance has been recognised in a thyroid hormone receptor deficit, whose gene (TRβ) has been mapped on chromosome 3p24.3 and several mutations have been identified. The clinical presentation may vary among a large spectrum from hypo-, to eu-, to hyperthyroidism in different patients, even in the same family. The diagnosis of RTH at birth and in the first months of life i…

HypothyroidismResistence to thyroid hormonesThyroid hormone receptors
researchProduct