Dersleri yüzünden oldukça stresli bir ruh haline sikiş hikayeleri bürünüp özel matematik dersinden önce rahatlayabilmek için amatör pornolar kendisini yatak odasına kapatan genç adam telefonundan porno resimleri açtığı porno filmini keyifle seyir ederek yatağını mobil porno okşar ruh dinlendirici olduğunu iddia ettikleri özel sex resim bir masaj salonunda çalışan genç masör hem sağlık hem de huzur sikiş için gelip masaj yaptıracak olan kadını gördüğünde porn nutku tutulur tüm gün boyu seksi lezbiyenleri sikiş dikizleyerek onları en savunmasız anlarında fotoğraflayan azılı erkek lavaboya geçerek fotoğraflara bakıp koca yarağını keyifle okşamaya başlar

GET THE APP

A Novel Synthetic LSD1 Inhibitor With Anticancer Activity In Prostate Cancer Cells | 106710

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

A novel synthetic LSD1 inhibitor with anticancer activity in prostate cancer cells

20th World Congress on Toxicology and Pharmacology

I-Chen Kung, Mei-Chuan Chen and Jing-Ping Liou

Taipei Medical University, Taiwan

Posters & Accepted Abstracts: Toxicol Open Access

Abstract
In United States during 2018 an estimated 164,690 new cases and 29,430 deaths of prostate cancer. Prostate cancer ranks as the first of new cases and the second of deaths from cancer in the US during 2018. The lysine-specific demethylase 1A (LSD1/KDM1A) is the first histone demethylase discovered and it can remove mono or di-methyl groups from lysine K4 or K9 on histone H3. LSD1 expression is increased in malignant prostate cancer. Overexpression of LSD1 enhances cell growth and cancer metastasis. Therefore, we want to treat prostate cancer by inhibiting cell growth or inducing cell death or suppressing cell migration and Epithelial???Mesenchymal Transition (EMT) through the inhibition of LSD1. We synthesized a new compound (Compound X) for LSD1 inhibition, and we compared with a well-known LSD1 inhibitor, SP2509. SP2509 can inhibit cell growth in prostate cancer cell PC3 and DU145 with micromolar GI50 value (1.34 and 2.12 ?M), and Compound X can inhibit cell growth in PC3 and DU145 with submicromolar GI50 value (0.34 and 0.89 ?M) by SRB assay. Our results showed that Compound X induces sub G1 phase of cell cycle arrest in a time-dependent manner and induces caspasedependent apoptosis and inhibits migration and EMT more than SP2509 in PC3 and DU145 cells. Knockdown of LSD1 enhances Compound X-induced cell apoptosis and suppression of migration in PC3 and DU145 cells. It has been reported that N-Myc Downstream-Regulated Gene 1 (NDRG1) is a potent metastatic suppressor in prostate and colon cancer cells. Our data showed that Compound X increase NDRG1 expression, therefore we will also investigate if NDRG1 plays an important role in the inhibition of migration and EMT by treated with Compound X. These data show that our new Compound X is more potent than well-known LSD1 inhibitor, SP2509.
Biography

I-Chen Kung has completed her graduation from the Department of Medical Laboratory Science and Biotechnology, Taipei Medical University. She is a Medical Technologist in Taiwan. She is currently pursuing her Masters in the Institute of Pharmacy, Taipei Medical University and also is a Member in the Clinical Drug Discovery Lab.

E-mail: s8039468@gmail.com

 

https://sekillinickyazma.com.tr/

Top