• 대한임상약리학회:학술대회논문집
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• 대한임상약리학회 1999년도 제8차 추계학술대회 및 정기총회
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• pp.48-48
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• 1999

• Biomolecules & Therapeutics
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• 제23권5호
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• pp.428-433
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• 2015

Acetylshikonin, a natural naphthoquinone derivative compound, has been used for treatment of inflammation and cancer. In the present study, we have investigated whether acetylshikonin could regulate the NF-${\kappa}B$ signaling pathway, thereby leading to suppression of tumorigenesis. We observed that acetylshikonin significantly reduced proliferation of several cancer cell lines, including human pancreatic PANC-1 cancer cells. In addition, acetylshikonin inhibited phorbol 12-myristate 13-acetate (PMA) or tumor necrosis-${\alpha}$ (TNF-${\alpha}$)-induced NF-${\kappa}B$ reporter activity. Proteome cytokine array and real-time RT-PCR results illustrated that acetylshikonin inhibition of PMA-induced production of cytokines was mediated at the transcriptional level and it was associated with suppression of NF-${\kappa}B$ activity and matrix metalloprotenases. Finally, we observed that an exposure of acetylshikonin significantly inhibited the anchorage-independent growth of PANC-1 cells. Together, our results indicate that acetylshikonin could serve as a promising therapeutic agent for future treatment of pancreatic cancer.

• Bulletin of the Korean Chemical Society
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• 제33권1호
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• pp.111-114
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• 2012

Androgen receptor (AR) is ligand-inducible nuclear hormone receptor which has been focused on key molecular target in growth and progression of prostate cancer. We synthesized a series of 4-aryl 2-substituted aniline-thiazole analogs and evaluated their anti-cancer activity in AR-dependent human prostate cancer LNCap cells. Among them, the compound 6 inhibited the tumor growth in LNCap-inoculated xenograft model.

• Biomolecules & Therapeutics
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• 제27권5호
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• pp.435-441
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• 2019

The capsaicin receptor TRPV1 (transient receptor potential vanilloid 1) has been an object of intense interest for pharmacological development on account of its critical role in nociception. In the course of structure activity analysis, it has become apparent that TRPV1 ligands may vary dramatically in the rates at which they interact with TRPV1, presumably reflecting differences in their abilities to penetrate into the cell. Using a fast penetrating agonist together with an excess of a slower penetrating antagonist, we find that we can induce an agonist response of limited duration and, moreover, the duration of the agonist response remains largely independent of the absolute dose of agonist, as long as the ratio of antagonist to agonist is held constant. This general approach for limiting agonist duration under conditions in which absolute agonist dose is variable should have more general applicability.

• Journal of Gastric Cancer
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• 제13권3호
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• pp.129-135
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• 2013

Gastric cancer is the second leading cause of cancer-related deaths worldwide. In advanced and metastatic gastric cancer, the conventional chemotherapy with limited efficacy shows an overall survival period of about 10 months. Patient specific and effective treatments known as personalized cancer therapy is of significant importance. Advances in high-throughput technologies such as microarray and next generation sequencing for genes, protein expression profiles and oncogenic signaling pathways have reinforced the discovery of treatment targets and personalized treatments. However, there are numerous challenges from cancer target discoveries to practical clinical benefits. Although there is a flood of biomarkers and target agents, only a minority of patients are tested and treated accordingly. Numerous molecular target agents have been under investigation for gastric cancer. Currently, targets for gastric cancer include the epidermal growth factor receptor family, mesenchymal-epithelial transition factor axis, and the phosphatidylinositol 3-kinase-AKT-mammalian target of rapamycin pathways. Deeper insights of molecular characteristics for gastric cancer has enabled the molecular classification of gastric cancer, the diagnosis of gastric cancer, the prediction of prognosis, the recognition of gastric cancer driver genes, and the discovery of potential therapeutic targets. Not only have we deeper insights for the molecular diversity of gastric cancer, but we have also prospected both affirmative potentials and hurdles to molecular diagnostics. New paradigm of transdisciplinary team science, which is composed of innovative explorations and clinical investigations of oncologists, geneticists, pathologists, biologists, and bio-informaticians, is mandatory to recognize personalized target therapy.

• Biomolecules & Therapeutics
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• 제11권4호
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• pp.205-213
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• 2003

Various angiogenesis inhibitors target vascular endothelial cells and block tumor angiogenesis. Angiostatin is a specific endogenous angiogenesis inhibitor in clinical trials, which contains only the first four triple loop structures, known as kringle domains. Its generated by proteolytic cleavage of its parent molecule plasminogen, which itself does not exhibit antiangiogenic activity. Kringle domains from prothrombin, apolipoprotein, hepatocyte growth factor, urokinase and tissue-type plasminogen activator also elicit anti-angiogenic or antitumor activities in several model systems, albeit low amino acid sequence identity between angiostatin and each individual kringle. However, the differential effects of each kringle domain on endothelial cell proliferation, and migration observed in these kringle domains, suggest that the amino acid sequence of the primary structure is still important although kringle architecture is essential for anti-mlgiogenic activity. If it is further studied as to how amino acid sequence and kringle architecture contributes in anti-angiogenic activity, with studies on underlying mechanisms of anti-angiogenesis by kringle-based angiogenesis inhibitors, it will provide basis for the development of new potent anti-angiogenesis inhibitors and improvement of the efficacy of angiogenesis inhibitors.

• Tuberculosis and Respiratory Diseases
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• 제47권6호
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• pp.797-806
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• 1999

연구배경: 소세포 폐암은 진단 당시 약 20% 이상에서 진단 당시 골수전이가 발견됨으로써 초기의 혈행성 전이가 중요한 예후인자일 것으로 추정되고 있다. 따라서 진단 또는 치료당시 기존의 검사수기로는 확인할 수 없었던 미세전이를 확인할 수 있다면 환자의 치료방침 및 예후결정에 유효한 지표가 될 수 있을 것으로 기대되어 왔다. 최근 cytokeratin(CK)-20 이 골수와 같은 조혈기관에서는 발현되지 않으면서 상피세포에서만 발현되는 것으로 알려져서 이 표지자가 소세포 폐암과 같은 상피세포암의 골수 미세전이의 발견에 효과적일 가능성을 사사하고 있다. 방 법: 소세포암세포주인 H209와 정상인의 혈구세포를 대상으로 CK-20 발현을 비교하였고, 소세포 폐암환자의 병기결정을 위한 경사로서 골수천자를 시행하면서 동시에 골수를 수집하여 이로부터 RNA를 수출하여 CK-20에 대한 primer를 이용하여 RT-PCR을 시행하였다. 결 과: H209 세포주에서는 CK-20의 발현이 관찰된 반면, 정상 혈구세포에서는 관찰되지 않아서 CK-20이 조혈세포에서는 발현되지 않고, 상피조직에 서만 특이적으로 발현되는 것으로 생각되었다. 28명의 소세포 폐암환자중 제한기가 11명, 확장기 환자가 17명이었으며, 17명의 확장기 환자가운데 골수조직검사상 골수 침범이 확인되었거나 또는 골주사검사상 전이가 확인된 환자는 7명(41%)이었다. CK-20에 대한 PCR 결과 각각 LD 11예종 l예(10%), ED 17예 중 1예(6%)에서 CK-20의 증폭이 관찰되었다. CK-20의 증폭이 관찰된 2예 중 ED 환자는 골수전이가 있었고, LD 환자는 진단당시는 원격전이가 없는 제한기의 환자였으나 후에 골전이가 관찰되었다. 결 론: 증폭이 관찰된 2 예의 환자가 모두 임상적으로는 골수 전이가 없는 상태에서 골전이가 발견됨으로써 CK-20의 발현이 혈행성 미세전이의 발견에 유용할 수 있을 가능성이 있을 것으로 추정할 수는 있으나, 골수전이가 확인되었던 7명중 6명에서는 CK-20이 발현되지 않아서, CK-20 보다 좀 더 유용한 표지자의 개발이 필요할 것으로 생각된다.

• Biomolecules & Therapeutics
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• 제15권3호
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• pp.133-136
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• 2007

Human papillomavirus (HPV) infection is the most common sexually transmitted disease in the United States. An estimated 6.2 million people are infected with HPV every year. Randomized controlled studies consistently show that HPV vaccine is effective in preventing infection and HPV related cervical lesions. In June 2006, Gardasil (qadrivalent HPV recombinant vaccine) was approved by the FDA for use in females 9-26 years of age. This article reviews published data to evaluate the effectiveness of HPV vaccine for the prevention of cervical cancer.

• 대한임상약리학회:학술대회논문집
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• 대한임상약리학회 2002년도 제11차 추계학술대회
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• pp.30-30
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• 2002

• Biomolecules & Therapeutics
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• 제30권6호
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• pp.479-489
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• 2022

5-Fluorouracil (5-FU) remains to be an important chemotherapeutic drug for treating several cancers when targeted therapy is unavailable. Chemoresistance limits the clinical utility of 5-FU, and new strategies are required to overcome the resistance. Reactive oxygen species (ROS) and antioxidants are balanced differently in both normal and cancer cells. Modulating ROS can be one method of overcoming 5-FU resistance. This review summarizes selected compounds and endogenous cellular targets modulating ROS generation to overcome 5-FU resistance.