Tamoxifen resistance

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  1. Mazepa Guest

    Tamoxifen resistance


    Farzana is currently doing a BMed Sci in the area of breast cancer research. She hopes to one day be an oncologist and clinician-scientist, and is looking forward to her final year of medical school in 2016. She plays violin in the Monash Medical Orchestra and enjoys devouring novels, travelling and spending time with her cat. The selective oestrogen receptor modulator (SERM), tamoxifen, is pivotal in treating oestrogen receptor positive (ER ) breast cancers—the most common subtype of breast cancer. As the first targeted therapy for breast cancer, tamoxifen remains the gold standard of adjuvant endocrine therapy. However, this important drug has its limitations: its efficacy is frequently hampered by the phenomenon of tamoxifen resistance. This article provides an overview of ER breast cancer biology relevant to understanding the complexities of tamoxifen resistance. The anti-oestrogen tamoxifen is the most commonly used treatment for patients with oestrogen-receptor (ER)-positive breast cancer. Although many patients benefit from tamoxifen in the adjuvant and metastatic settings, resistance is an important clinical problem. Over the last decade many advances have been made in our understanding of the biology of the ER which may help to explain how resistance to tamoxifen develops. Such mechanisms may include changes in the expression of ERα or ERβ, alterations in co-regulatory proteins, and the influences of cellular kinase signal transduction pathways. The experimental and clinical evidence supporting these mechanisms of tamoxifen resistance are discussed in this review. The anti-oestrogen tamoxifen is the most commonly used treatment for patients with oestrogen-receptor (ER)-positive breast cancer. Although many patients benefit from tamoxifen in the adjuvant and metastatic settings, resistance is an important clinical problem. Over the last decade many advances have been made in our understanding of the biology of the ER which may help to explain how resistance to tamoxifen develops. Such mechanisms may include changes in the expression of ERα or ERβ, alterations in co-regulatory proteins, and the influences of cellular kinase signal transduction pathways.

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    Emerging knowledge on the molecular mechanisms of tamoxifen resistance will provide insight into the design of regimens to overcome tamoxifen resistance. Better understanding of these mechanisms may suggest novel strategies to overcome tamoxifen resistance and make further improvements in breast cancer. Sep 23, 2015. Now, scientists have traced out an intricate molecular pathway in those cells they say may explain, at least in part, how tamoxifen resistance.

    Abnormal uterine bleeding (AUB) is one of the most common presenting complaints encountered in a gynecologist’s office or primary care setting. An estimated 60% of visits to a physician’s office are from women seeking treatment for menstrual problems. Unpredictable and unscheduled bleeding often lead to psychological, medical, and sexual problems requiring pharmacologic and surgical interventions. Hysterectomy is the second most common surgery performed in the United States, with 500,000–600,000 hysterectomies performed per annum at a cost of over $ 2 billion. The intent of this chapter is to review the etiology, evaluation, diagnosis, and medical and surgical management of AUB in women during midlife. Dysfunctional uterine bleeding (DUB) is defined as AUB with no demonstrable organic genital or extragenital cause. More than 50% of hysterectomies performed for excessive blood loss have no abnormal pathologic evaluation. This summary discusses primary epithelial breast cancers in women. The breast is rarely affected by other tumors such as lymphomas, sarcomas, or melanomas. Refer to the following PDQ summaries for more information on these cancer types: disease and 268,600 cases of invasive disease in 2019.[1] Thus, fewer than one of six women diagnosed with breast cancer die of the disease. By comparison, it is estimated that about 66,020 American women will die of lung cancer in 2019.[1] Men account for 1% of breast cancer cases and breast cancer deaths (refer to the Special Populations section in the PDQ summary on Breast Cancer Screening for more information). Widespread adoption of screening increases breast cancer incidence in a given population and changes the characteristics of cancers detected, with increased incidence of lower-risk cancers, premalignant lesions, and ductal carcinoma (DCIS). (Refer to the Ductal carcinoma in situ (DCIS) section in the Pathologic Evaluation of Breast Tissue section in the PDQ summary on Breast Cancer Screening for more information.) Population studies from the United States [2] and the United Kingdom [3] demonstrate an increase in DCIS and invasive breast cancer incidence since the 1970s, attributable to the widespread adoption of both postmenopausal hormone therapy and screening mammography. In the last decade, women have refrained from using postmenopausal hormones, and breast cancer incidence has declined, but not to the levels seen before the widespread use of screening mammography.[4] Age-specific risk estimates are available to help counsel and design screening strategies for women with a family history of breast cancer.[22,23] Of all women with breast cancer, 5% to 10% may have a germline mutation of the genes mutation has been identified, other family members can be referred for genetic counseling and testing.[29-32] (Refer to the PDQ summaries on Genetics of Breast and Gynecologic Cancers; Breast Cancer Prevention; and Breast Cancer Screening for more information.) (Refer to the PDQ summary on Breast Cancer Prevention for more information about factors that increase the risk of breast cancer.) Clinical trials have established that screening asymptomatic women using mammography, with or without clinical breast examination, decreases breast cancer mortality.

    Tamoxifen resistance

    Strategies to overcome tamoxifen resistance in breast cancer., Mechanisms of tamoxifen resistance in Endocrine-Related Cancer.

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  7. Tamoxifen C26H29NO CID 2733526 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety.

    • Tamoxifen C26H29NO - PubChem.
    • Molecular 'feedback loop' may explain tamoxifen resistance in patients..
    • P-glycoprotein - Wikipedia.

    Le tamoxifène est un modulateur sélectif des récepteurs des œstrogènes utilisé sous forme orale dans le cancer du sein. Il est pour l'instant le traitement le. Tamoxifen has been used for the systemic treatment of patients with breast cancer by block the action of estrogen is also used to lower a woman's chance of. Tamoxifen, sold under the brand name Nolvadex among others, is a medication that is used to prevent breast cancer in women and treat breast cancer in women and men.

     
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