Biochemical pharmacology

Biochem Pharmacol · ISSN (e) 1873-2968 · 18 papers in corpus
article 2024
doi:10.1016/j.bcp.2024.116280 ·PMID:38735446

The pivotal role of human endometrial stromal cells (hESCs) in the development of endometriosis lies in their ability to adopt a pro-invasive and proinflammatory profile upon migration to areas outside the uterus. However, the molecular mec…

review 2024
doi:10.1016/j.bcp.2024.116565 ·PMID:39368751

Carnitine is a vital molecule in human metabolism, prominently involved in fatty acid β-oxidation within mitochondria. Predominantly sourced from dietary intake, carnitine also derives from endogenous synthesis. This review delves into the …

2023
doi:10.1016/j.bcp.2023.115552 ·PMID:37068524

Estrogen Receptor is the driving transcription factor in about 75% of all breast cancers, which is the target of endocrine therapies, but drug resistance is a common clinical problem. ESR1 point mutations at the ligand binding domain are fr…

2022
doi:10.1016/j.bcp.2021.114848 ·PMID:34801523

Exposure to naturally derived estrogen receptor activators, such as the phytoestrogen genistein, can occur at physiologically relevant concentrations in the human diet. Soy-based infant formulas are of particular concern because infants con…

2021
doi:10.1016/j.bcp.2020.114300 ·PMID:33203518

Geoffrey Burnstock, the founder of the field of purinergic signaling research passed away in Melbourne, Australia on June 3rd, 2020, at the age of 91. With his death, the world of biomedical research lost one of its most passionate, creativ…

2021
doi:10.1016/j.bcp.2020.114311 ·PMID:33130128

Prof. Geoffrey Burnstock originated the concept of purinergic signaling. He demonstrated the interactions and biological roles of ionotropic P2X and metabotropic P2Y receptors. This review paper traces the historical origins of many current…

2021
doi:10.1016/j.bcp.2020.114310 ·PMID:33130130

During the molecular transduction of itch, the stimulation of pruriceptors on sensory fibers leads to the activation or sensitization of ion channels, which results in a consequent depolarization of the neurons. These ion channels mostly be…

2020
doi:10.1016/j.bcp.2020.114129 ·PMID:32619425

Neuropeptides are signalling molecules mainly secreted from neurons that act as neurotransmitters or peptide hormones to affect physiological processes and modulate behaviours. In humans, neuropeptides are implicated in numerous diseases an…

2017
doi:10.1016/j.bcp.2017.08.004 ·PMID:28800957

17β-Hydroxysteroid dehydrogenase type 1 (17β-HSD1) is involved in the biosynthesis of estradiol, the major bioactive endogenous estrogen in mammals, and constitutes an interesting therapeutic target for estrogen-dependent diseases. A steroi…

article 2016
doi:10.1016/j.bcp.2016.03.024 ·PMID:27038655

Hexachlorobenzene (HCB) is an organochlorine pesticide that induces toxic reproductive effects in laboratory animals. It is a dioxin-like compound and a weak ligand of the aryl hydrocarbon receptor (AhR). Endometriosis is characterized by t…

2013
doi:10.1016/j.bcp.2013.06.030 ·PMID:23856290

Pregnancy is associated with uteroplacental and vascular remodeling in order to adapt for the growing fetus and the hemodynamic changes in the maternal circulation. We have previously shown upregulation of uterine matrix metalloproteinases …

article 2011
doi:10.1016/j.bcp.2011.12.030 ·PMID:22227273

The disease of reproductive women, endometriosis represents implantation of functional endometrial glands outside uterine cavity. This invasive disorder is associated with dysregulation of matrix metalloproteases (MMP)s and extracellular ma…

2011
doi:10.1016/j.bcp.2011.08.026 ·PMID:21924251

Estrogen signaling is mediated by two estrogen receptors (ERs), ERα and ERβ, which have unique roles in the regulation of breast cancer cell proliferation. ERα induces proliferation in response to estrogen and ERβ inhibits proliferation in …

other 2009
doi:10.1016/j.bcp.2008.10.016 ·PMID:19013437

Progesterone receptor (PR) modulators are used in contraception and post-menopausal hormone therapy, and are under clinical development for reproductive disorders such as uterine fibroids and endometriosis. Development of tissue selective P…

2009
doi:10.1016/j.bcp.2008.09.016 ·PMID:18848529

The AHR is well known for regulating responses to an array of environmental chemicals. A growing body of evidence supports the hypothesis that the AHR also plays perhaps an even more important role in modulating critical aspects of cell fun…

2009
doi:10.1016/j.bcp.2008.09.031 ·PMID:18940186

The aryl hydrocarbon receptor (AhR) is an orphan receptor in the basic helix-loop-helix PAS family of transcriptional regulators. Although the endogenous regulator of this pathway has not been identified, the AhR is known to bind and be act…

2008
doi:10.1016/j.bcp.2007.07.004 ·PMID:17678629

Matrix metalloproteinases (MMPs) are a family of proteolytic enzymes that degrade various components of the extracellular matrix (ECM). Members of the MMP family include collagenases, gelatinases, stromelysins, matrilysins and membrane-type…

review 1998
doi:10.1016/s0006-2952(98)00074-4 ·PMID:9744562

The word antioxidant has become a household term, and every day we are bombarded with claims of antioxidant protection against a host of diseases. Atherosclerosis, cancer, gastric ulcers, memory loss, rheumatoid arthritis, endometriosis, pr…