권영주 교수
Young Ju Kwon
고려대학교 내과 · 의학
연구실 소개
권영주 교수의 연구실은 암 치료를 위한 새로운 약물 후보 물질 개발과 간 섬유화 등 만성 질환의 분자 기전 규명을 핵심으로 삼고 있습니다. 특히 트리플네거티브유방암의 표적 치료제로 활용 가능한 테르피리딘 유도체 및 토포이소머라제 억제제를 설계하고, 간성 활성화된 성상세포를 표적으로 하는 나노입자 기반 치료 전략을 개발하고 있습니다. 또한, 유전자 발현 조절을 위한 인공 전사인자 설계와 같은 분자생물학적 접근도 병행하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Breast cancer accounts for 25% of all types of cancer in women, and triple negative breast cancer (TNBC) comprises around 15~20% of breast cancers. Conventional chemotherapy and radiation are the primary systemic therapeutic strategies; no other FDA-approved targeted therapies are yet available as for TNBC. TNBC is generally characterized by a poor prognosis and high rates of proliferation and metastases. Due to these aggressive features and lack of targeted therapies, numerous attempts have bee
A series of novel terpyridine-skeleton molecules containing conformational rigidity, 14 containing benzo[4,5]furo[3,2-b]pyridine core and 15 comprising chromeno[4,3-b]pyridine core, were synthesized, and their biological activities were evaluated. 3-(4-Phenylbenzo[4,5]furo[3,2-b]pyridin-2-yl)phenol (8) was determined to be a nonintercalative topo I and II dual catalytic inhibitor and 3-(4-phenylchromeno[4,3-b]pyridine-2-yl)phenol (22) was determined to be a nonintercalative topo IIα specific cat
Liver fibrosis is a life-threatening and irreversible disease. The fibrosis process is largely driven by hepatic stellate cells (HSCs), which undergo transdifferentiation from an inactivated state to an activated one during persistent liver damage. This activated state is responsible for collagen deposition in liver tissue and is accompanied by increased CD44 expression on the surfaces of HSCs and amplified intracellular oxidative stress, which contributes to the fibrosis process. To address thi
Regulation of gene expression by transcription factors touches many aspects of eukaryotic biology, and its systematic, external control by organic molecules represents a challenge in chemistry. Here we report the design of a completely organic, nonpeptidic compound that mimics a transcription factor. The design takes advantage of the specific DNA-binding affinity of a hairpin polyamide molecule and the ability of wrenchnolol to bind to the Sur-2 subunit of human mediator complex. The hybrid comp
This study based on the person-environment fit theory, giving a definition of job stress. Job stress is defined as unfit between person and environment and type of unfit is classified need-supplies unfit and abilities-demand unfit. Using this concept as a basis, it is analysed that social support type moderates teachers' burnout according to job stressors. The results indicate that social supports have a buffering effects or reverse buffering effect according to interaction of job stressors and
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