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Journal of Clinical & Experimental Pathology | ISSN: 2161-0681 | Volume 8

Breast Pathology and Cancer Diagnosis

6

th

World Congress and Expo on

July 25-26, 2018 | Vancouver, Canada

Medicinal Chemistry and Rational Drugs

20

th

International Conference on

&

Correction of a scientific error in lippincott illustrated reviews pharmacology (anticancer drugs, p 605,

Mechanism of action

of tamoxifen)

Hussein Albarazanchi

Kurdistan Institute for Strategic Studies and Scientific Research-Cancer, Iraq

T

amoxifen is one of the selective estrogen receptor modulators (SERM) with tissue-specific activities for the treatment

and prevention of estrogen receptor positive breast cancer. Tamoxifen acts as an anti-estrogen (inhibiting agent) in the

mammary tissue, but as an estrogen (stimulating agent) in cholesterol metabolism, bone density, and cell proliferation in the

endometrium.

Mechanism of Action:

Tamoxifen is a nonsteroidal agent that binds to estrogen receptors (ER), inducing a conformational

change in the receptor. This results in a blockage or change in the expression of estrogen dependent genes. The prolonged

binding of tamoxifen to the nuclear chromatin of these results in reduced DNA polymerase activity, impaired thymidine

utilization, blockade of estradiol uptake, and decreased estrogen response. It is likely that tamoxifen interacts with other

coactivators or corepressors in the tissue and binds with different estrogen receptors, ER-alpha or ER-beta, producing both

estrogenic and antiestrogenic effects.

The illustration on the mechanism of action of tamoxifen in the book as follow:

B. Tamoxifen:

Tamoxifen [tah-MOX-ih-fen] is an estrogen antagonist with some estrogenic activity, and it is classified as a

selective estrogen receptor modulator (SERM). It is used for first-line therapy in the treatment of estrogen receptor–positive

breast cancer. It also finds use prophylactically in reducing breast cancer occurrence in women who are at high risk. However,

because of possible stimulation of premalignant lesions due to its estrogenic properties, patients should be closely monitored

during therapy.

Mechanism of action:

Tamoxifen binds to estrogen receptors in the breast tissue, but the complex is unable to translocate into

the nucleus for its action of initiating transcriptions. That is, the complex fails to induce estrogen-responsive genes, and RNA

synthesis does not ensue (Figure 46.26B). The result is a depletion (down-regulation) of estrogen receptors, and the growth-promoting.

The error is highlighted with yellow color, the correction is as follow:

Tamoxifen binds to estrogen receptors in the breast tissue, but the complex not productive, the complex fails to induce estrogen-

responsive genes and RNA synthesis does not ensue. That is mean, the complex enter the nucleus, while its action block on the

gene and prevent the translation effects of estrogen.

Biography

Hussein Albarazanchi born in Iraq, 1977, has

M.Sc

. cancer pharmacology from university of Bradford-institute of cancer therapeutics, and also has Bachelor

degree in veterinary medicine and surgery from college of veterinary medicine-university of sulaimani-Kurdistan of Iraq. Currently he is working as a researcher in

Kurdistan institute for strategic studies and scientific research-cancer research Dept., Kurdistan of Iraq; and as a lecturer of anticancer drugs in college of pharmacy

university of sulaimani.

Hussein.al-barazanchi@kissr.edu.krd

Hussein Albarazanchi, J Clin Exp Pathol 2018, Volume 8

DOI: 10.4172/2161-0681-C3-052