Evaluate the inhibition of cytochrome P450 1A1 for enhancing breast cancer chemotherapy with a turn-on fluorescent probe

نویسندگان

چکیده

The incidence rate of breast cancer ranks first in women malignant tumors worldwide, accompanied by a high mortality. early diagnosis and therapy are important way to reduce the mortality clinical practice. There urgent needs for anti-tumor strategies with clear evidence reliable efficacy. Because cytochrome P450 1A1 (CYP1A1) is commonly expressed has excellent ability metabolize xenobiotics, researchers interested studying vital function CYP1A1 cancer. Herein, we report BCy-CYP fluorescent probe imaging cells vivo. This outstanding selectivity sensitivity detection over other biomolecules. Our results reveal that intracellular level increase MCF-7 MDA-MB-231 cells, inhibition carnosol efficiently induce apoptosis two kinds cells. Thus, plays crucial role synergistic effect chemotherapy drug better than alone tumor-bearing mice. may be new biomarker diagnosis.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Study of Cytochrome P450 1A1 (T3801C) Single Nucleotide Polymorphism in Patients with Breast Cancer in Mazandaran Province-Northern Iran

 Background: Breast cancer is the first leading cause of cancer-related death in women. Pesticides which are excessively used in northern Iran are one of the most important risk factors for breast cancer incidence. The cytochrome P450 1A1 (cyp1A1) is a key enzyme in xenobiotics metabolism and SNPs of its coding gene has been verified to be important in cancer susceptibility. The aim of thi...

متن کامل

Methoxyestrogens exert feedback inhibition on cytochrome P450 1A1 and 1B1.

Cytochrome P450 1A1 (CYP1A1) and 1B1 (CYP1B1) catalyze the oxidative metabolism of 17 beta-estradiol (E2) to catechol estrogens (2-OHE2 and 4-OHE2) and estrogen quinones, which may lead to DNA damage. Catechol-O-methyltransferase catalyzes the methylation of catechol estrogens to methoxyestrogens (2-MeOE2, 2-OH-3-MeOE2, and 4-MeOE2), which simultaneously lowers the potential for DNA damage and ...

متن کامل

Mechanism-based inhibition of human cytochrome P450 1A1 by rhapontigenin.

Recently we reported that resveratrol (trans-3,4',5-trihydroxystilbene) showed selective inhibition of recombinant human cytochrome P450 (P450) 1A1 in a concentration-dependent manner. The inhibition of recombinant human P450 1A1, 1A2, or 1B1 by various hydroxystilbene compounds having a similar structure to resveratrol was investigated using bacterial membranes from a human P450/NADPH-P450 red...

متن کامل

study of cytochrome p450 1a1 (t3801c) single nucleotide polymorphism in patients with breast cancer in mazandaran province-northern iran

background: breast cancer is the first leading cause of cancer-related death in women. pesticides which are excessively used in northern iran are one of the most important risk factors for breast cancer incidence. the cytochrome p450 1a1 (cyp1a1) is a key enzyme in xenobiotics metabolism and snps of its coding gene has been verified to be important in cancer susceptibility. the aim of this stud...

متن کامل

Polymorphism of the cytochrome P-450 1A1 (A2455G) in women with breast cancer in Eastern Azerbaijan, Iran

Objective(s):Cytochrome P-450 1A1 is an important enzyme in the first phase of the metabolism of some carcinogens such as polycyclic aromatic hydrocarbons (PAHs), as well as estrogen. The present study evaluates the existence of CYP1A1 polymorphism in a number of breast cancer samples. Materials and Methods: One hundred breast cancer patients and the same number of healthy controls were analyz...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Sensors and Actuators B-chemical

سال: 2021

ISSN: ['0925-4005', '1873-3077']

DOI: https://doi.org/10.1016/j.snb.2021.130233