서재홍 교수
Jae Hong Seo
고려대학교 내과 · 의학
연구실 소개
서재홍 교수의 연구실은 유방암의 면역 미세환경과 종양 생물학적 특성 간의 상관관계를 중심으로, T세포, 조절성 T세포(Foxp3+ Tregs) 등 면역세포의 역할을 규명하고 있습니다. 특히 삼중음성 유방암(TNBC)에 대한 새로운 표적치료제 개발을 목표로 하며, HSP90 억제제 SL-145의 Apoptosis 유도 기전과 열충격 반응 유도 여부에 대한 기전적 연구를 진행하고 있습니다. 또한, 위암 및 유방암 환자의 혈액에서 종양 마커 mRNA를 모니터링하여 조기 재발 예측 가능성을 탐색하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15BACKGROUND: The balance in the immune system between immune surveillance against non-self-antigens and tolerance of self-antigens is known to be associated with the prognosis of breast cancer patients. However, immunologic signals in tumor microenvironment according to biological characteristics of cancer cells have not been clearly elucidated. CD4(+) T cells, CD8(+) T cells, and forkhead box P3-positive (Foxp3) regulatory T cells (Tregs) are the main keys for immune surveillance and tolerance,
In order to evaluate the role of BRCA1 and BRCA2 germline mutations in Korean patients with sporadic breast cancer, 97 patients with sporadic breast cancer were analyzed for mutations in the BRCA1 and BRCA2 coding regions, by using a combination of fluorescent-conformation sensitive gel electrophoresis (F-CSGE) and direct sequencing. Fifty-five distinct sequence variants were detected, which included three pathogenic truncating mutations, 15 missense mutations, 16 polymorphisms, and 21 intronic
Some suggestive but not entirely consistent nor conclusive evidence was found on the association between the history of preeclampsia or PIH with the subsequent risk of breast cancer.
Despite recent advances, there remains a significant unmet need for the development of new targeted therapies for triple-negative breast cancer (TNBC). Although the heat shock protein HSP90 is a promising target, previous inhibitors have had issues during development including undesirable induction of the heat shock response (HSR) and off-target effects leading to toxicity. SL-145 is a novel, rationally-designed C-terminal HSP90 inhibitor that induces apoptosis in TNBC cells via the suppression
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