• 제목/요약/키워드: Anti-Cancer Activities

검색결과 717건 처리시간 0.031초

Synthesis of Flavokawain Analogues and their Anti-neoplastic Effects on Drug-resistant Cancer Cells Through Hsp90 Inhibition

  • Seo, Young Ho;Park, Sun You
    • Bulletin of the Korean Chemical Society
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    • 제35권4호
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    • pp.1154-1158
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    • 2014
  • Hsp90 is an ubiquitous molecular chaperone protein, which plays an important role in regulating maturation and stabilization of many oncogenic proteins. Due to its potential to simultaneously disable multiple signaling pathways, Hsp90 represents great promise as a therapeutic target of cancer. In this study, we synthesized flavokawain analogues and evaluated their biological activities against drug-resistant cancer cells. The study indicated that compound 1i impaired the growth of gefitinib-resistant non-small cell lung cancer (H1975), down-regulated the expression of Hsp90 client proteins including EGFR, Her2, Met, Akt and Cdk4, and upregulated the expression of Hsp70. The result strongly suggested that compound 1i inhibited the proliferation of cancer cells through Hsp90 inhibition. Overall, compound 1i could serve as a potential lead compound to overcome the drug resistance in cancer chemotherapy.

감귤과 녹차의 추출액으로 제조한 콤부차의 생리 활성 및 일반 세포 독성 (Bioactivity and Cytotoxicity of Kombucha Fermented with Extracts from Green Tea and Citrus Peel)

  • 신승식;고혜명;김청이;박성수
    • 한국식품영양과학회지
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    • 제45권12호
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    • pp.1838-1842
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    • 2016
  • 콤부차는 미생물의 공생체에 의해 제조되는 신맛이 강한 음료로 최근에는 "장수 식품"의 하나로 주로 러시아를 비롯한 서방 국가들에서 많이 음용되어온 기능성 음료이다. 본 연구에서는 일반적으로 제조되는 콤부차의 기능성을 제주 특산물인 감귤의 과피 추출액과 녹차의 추출액을 첨가한 후 콤부차를 발효시켜 각 성분이 가지는 기능성을 이행시킬 목적으로 감귤/녹차 콤부차를 제조하였고, 제조된 감귤/녹차 콤부차의 기능성을 항암성 중심으로 일반 콤부차와 비교 평가하였다. 또한, 콤부차의 산업화, 표준화 및 안전성 확보를 위하여 일반 세포에 미치는 독성의 정도를 RAW 264.7 마우스 대식세포를 이용하여 조사하였다. 그 결과 일반 콤부차보다 감귤/녹차 콤부차는 항산화력이 약 3배 증가하였으며, 항암성도 현저하게 증가한 것으로 나타났다. 특히 일반 세포에 대한 독성은 현저히 낮아진 것으로 나타났으며, 이는 감귤/녹차 콤부차의 안전한 항암 기능성 음료로의 개발 가능성을 시사하고 있다.

Paclitaxel, Lenvatinib 및 방사선 병용 요법의 역형성 갑상선암에서의 항암 작용 (Anti-cancer Activity of Paclitaxel, Lenvatinib and Radiation Combination Therapy on Anaplastic Thyroid Cancer in Vitro and in Vivo)

  • 전시열;김수영;김석모;박기청;김희준;장호진;이용상;장항석;박정수
    • 대한두경부종양학회지
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    • 제35권2호
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    • pp.19-25
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    • 2019
  • Background/Objectives: Although anaplastic thyroid carcinoma (ATC) is rare, it is one of the deadliest forms of thyroid cancer. The fatality rate for ATC is high, and the survival rate at one year after diagnosis is <20%. The present study aimed to investigate the anti-tumor activities of paclitaxel, radiation, and tyrosine kinase inhibitor (TKI) combined therapy in anaplastic thyroid cancer cells both in vitro and in vivo and explore its effects on apoptotic cell death pathways. Materials & Methods: ATC cell line was exposed to TKI, lenvatinib in the presence or absence of paclitaxel with radiation, and cell viability was determined by MTT assay. Effects of the combined treatment on cell cycle and intracellular signaling pathways were assessed by flow cytometry and western blot analysis. The ATC cell line xenograft model was used to examine the anti-tumor activity in vivo. Results: Our data revealed that the combined administration of paclitaxel, TKI, and radiation decreased cell viability in ATC cells, and also significantly increased apoptotic cell death in these cells, as demonstrated by the cleavage of caspase-3 and DNA fragmentation. This combination therapy reduced anti-apoptotic factor levels in ATC cells, while significantly decreasing tumor volume and increasing survival in ATC xenografts. Conclusion: These results indicate that administering the combination of paclitaxel, TKI, and radiation therapy may exert significant anticancer effects in preclinical models, potentially suggesting a new clinical approach for treating patients with ATC.

Anticoagulant activities of oleanolic acid via inhibition of tissue factor expressions

  • Lee, Won-Hwa;Yang, Eun-Ju;Ku, Sae-Kwang;Song, Kyung-Sik;Bae, Jong-Sup
    • BMB Reports
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    • 제45권7호
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    • pp.390-395
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    • 2012
  • Oleanolic acid (OA), a triterpenoid known for its anti-inflammatory and anti-cancer properties, is commonly present in several medicinal plants but its anticoagulant activities have not been studied. Here, the anticoagulant properties of OA were determined by monitoring activated partial thromboplastin time (aPTT), prothrombin time (PT), fibrin polymerization as well as cell-based thrombin and activated factor X (FXa) generation activities. Data showed OA prolonged aPTT and PT significantly and inhibited thrombin catalyzed fibrin polymerization. In addition, OA inhibited the activities of thrombin and FXa and inhibited the generation of thrombin or FXa in human endothelial cells. OA also inhibited TNF-${\alpha}$-induced tissue factor expression on human endothelial cells. In accordance with these anticoagulant activities, OA showed an anticoagulant effect in vivo. These results indicate that OA possesses antithrombotic activities and suggest that daily consumption of a herb containing OA may be preventing thrombosis in pathological states.

Diethyldithiocarbamate Suppresses an NF-κB Dependent Metastatic Pathway in Cholangiocarcinoma Cells

  • Srikoon, Pattaravadee;Kariya, Ryusho;Kudo, Eriko;Goto, Hiroki;Vaeteewoottacharn, Kulthida;Taura, Manabu;Wongkham, Sopit;Okada, Seiji
    • Asian Pacific Journal of Cancer Prevention
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    • 제14권7호
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    • pp.4441-4446
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    • 2013
  • Cholangiocarcinoma (CCA) is a tumor of biliary ducts, which has a high mortality rate and dismal prognosis. Constitutively activation of the transcription factor nuclear factor kappa-B (NF-${\kappa}B$) has been previously demonstrated in CCA. It is therefore a potential target for CCA treatment. Effects of diethyldithiocarbamate (DDTC) on NF-${\kappa}B$-dependent apoptosis induction in cancer have been reported; however, anti-metastasis has never been addressed. Therefore, here the focus was on DDTC effects on CCA migration and adhesiond. Anti-proliferation, anti-migration and anti-adhesion activities were determined in CCA cell lines, along with p65 protein levels and function. NF-${\kappa}B$ target gene expression was determined by quantitative RT-PCR. DDTC inhibited CCA cell proliferation. Suppression of migration and adhesion were observed prior to anti-CCA proliferation. These effects were related to decreased p65, reduction in NF-${\kappa}B$ DNA binding, and impaired activity. Moreover, suppression of ICAM-1 expression supported NF-${\kappa}B$-dependent anti-metastatic effects of DDTC. Taken together, DDTC suppression of CCA migration and adhesion through inhibition of NF-${\kappa}B$ signaling pathway is suggested from the current study. This might be a promising treatment choice against CCA metastasis.

정금나무의 기능성 생리활성 물질과 생리활성 (Functional Bioactive Compounds and Biological Activities of Vaccinium oldhamii)

  • 채정우;조희선
    • 생명과학회지
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    • 제32권2호
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    • pp.167-174
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    • 2022
  • 현대사회에서 산화물질에 의한 스트레스가 증가함에 따라 항산화제에 대한 관심이 증가하고 있다. 그러나 합성 항산화제는 다량 섭취 시 유해하다는 연구 등에 기인하여 수요가 감소하고 있으며, 합성 항산화제를 대체하기 위하여 천연물에서 유래된 항산화 물질에 관한 연구가 활발히 진행되고 있다. 세계 10대 장수 식품의 하나로 알려진 블루베리는 진달래과(Ericaceae) 산앵도나무속(Vaccinium)의 식물로 항산화를 비롯한 다양한 약리활성에 대한 연구가 수행되었다. 정금나무(Vaccinium oldhamii)는 블루베리와 같은 속에 속한 낙엽활엽관목으로 본 논문에서는 정금나무의 추출물과 정제물의 효능 분석을 실시한 연구들을 정리하였다. 정금나무 열매의 페놀류 화합물의 함량은 항산화 활성 및 항인플루엔자 활성과 비례하였으며, 총 폴리페놀 및 안토시아닌의 함량은 블루베리에 비해 높았다. 정금나무 열매 추출물은 항염증 활성을 나타내었으며 정금나무 가지 추출물은 항염증 활성과 염증반응에 의한 파골세포의 분화 및 골흡수를 억제하는 활성을 나타내었다. 정금나무 열매 추출물은 인간 급성 백혈병에 대한 항암 활성을, 정금나무 가지 추출물은 여러 인간 암세포주에서의 항암활성을 나타내었다. 정금나무는 블루베리에 비하여 페놀성 화합물 함량과 항산화 활성이 높고 다양한 생리활성을 나타내며, 국내에 자생하여 대량 재배를 위한 연구가 용이하고, 상업화 시 해외 사용료를 부담할 필요가 없는 등 블루베리의 대체작물로서의 가치를 충분히 가지고 있다고 판단된다.

MCF-7 유방암 세포에서 영릉향 추출물에 의한 Apoptosis 유도에 관한 연구 (The Extract from Lysimachia foenum-graecum Induces Apoptosis in MCF-7 Breast Cancer Cells)

  • 이세희;김근태;김종일;임은경;김인섭;김영민
    • KSBB Journal
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    • 제28권5호
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    • pp.303-309
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    • 2013
  • The extract from Lysimachia foenum-graecum (LFE) has been known to possess various instructive characters including anti-oxidant, anti-obesity, fungicidal activities. However, the accurate mechanism of those effects of LFE is not well known. In that respect, we evaluated the apoptotic effect and anti-cancer efficacy of extracts of LFE in MCF-7 breast cancer cells. In this study, we hypothesized that LFE may exert cancer cell apoptosis through regulating p53 and mitochondria-mediated apoptotic proteins. And this substance can generate ROS to cause free radical-induced apoptosis. Accordingly, the generation of ROS by LFE triggers the activation of p53 which are accompanied by pro-apoptotic protein activation and suppression of pro-survival proteins. We determined with MTT assay, flow cytometry for detection of intracellular ROS and Annexin V-PI staining, Western blotting. Consequently, our researches demonstrated that the treatment of LFE to breast cancer cells resulted in an activation of p53, Puma, Bax, cleaved-PARP and an inhibition of Bcl-2 expressions.

Anti-tumor activities of Panax quinquefolius saponins and potential biomarkers in prostate cancer

  • He, Shan;Lyu, Fangqiao;Lou, Lixia;Liu, Lu;Li, Songlin;Jakowitsch, Johannes;Ma, Yan
    • Journal of Ginseng Research
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    • 제45권2호
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    • pp.273-286
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    • 2021
  • Background: Prostate carcinoma is the second most common cancer among men worldwide. Developing new therapeutic approaches and diagnostic biomarkers for prostate cancer (PC) is a significant need. The Chinese herbal medicine Panax quinquefolius saponins (PQS) have been reported to show anti-tumor effects. We hypothesized that PQS exhibits anti-cancer activity in human PC cells and we aimed to search for novel biomarkers allowing early diagnosis of PC. Methods: We used the human PC cell line DU145 and the prostate epithelial cell line PNT2 to perform cell viability assays, flow cytometric analysis of the cell cycle, and FACS-based apoptosis assays. Microarray-based gene expression analysis was used to display specific gene expression patterns and to search for novel biomarkers. Western blot and quantitative real-time PCR were performed to demonstrate the expression levels of multiple cancer-related genes. Results: Our data showed that PQS inhibited the viability of DU145 cells and induced cell cycle arrest at the G1 phase. A significant decrease in DU145 cell invasion and migration were observed after 24 h treatment by PQS. PQS up-regulated the expression levels of p21, p53, TMEM79, ACOXL, ETV5, and SPINT1 while it down-regulated the expression levels of bcl2, STAT3, FANCD2, DRD2, and TMPRSS2. Conclusion: PQS promoted cells apoptosis and inhibited the proliferation of DU145 cells, which suggests that PQS may be effective for treating PC. TMEM79 and ACOXL were expressed significantly higher in PNT2 than in DU145 cells and could be novel biomarker candidates for PC diagnosis.

Loquat (Eriobotrya japonica) extracts suppress the adhesion, migration and invasion of human breast cancer cell line

  • Kim, Min-Sook;You, Mi-Kyoung;Rhuy, Dong-Young;Kim, Yung-Jae;Baek, Hum-Young;Kim, Hyeon-A
    • Nutrition Research and Practice
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    • 제3권4호
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    • pp.259-264
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    • 2009
  • We examined the inhibitory effects of loquat methanol extract on the adhesion, migration, invasion and matrix metalloproteinase (MMP) activities of MDA-MB-231 human breast cancer cell line. Cells were cultured with DMSO or with 10, 25, or 50 ${\mu}g/ml$ of loquat methanol extract. Both leaf and seed extracts significantly inhibited growth of MDA-MB-231 cells in a dose-dependent manner, although leaf extract was more effective. Adhesion and migration were significantly inhibited by loquat extracts in a dose-dependent manner. Loquat extract also inhibited the invasion of breast cancer cells in a dose-dependent manner and leaf extract was more effective than seed extract. MMP-2 and MMP-9 activities were also inhibited by loquat extract. Our results indicate that methanol extracts of loquat inhibit the adhesion, migration and invasion of human breast cancer cells partially through the inhibition of MMP activity and leaf extract has more anti-metastatic effects in cell based assay than seed extract. Clinical application of loquat extract as a potent chemopreventive agent may be helpful in limiting breast cancer invasion and metastasis.

Biphasic Activity of Chloroquine in Human Colorectal Cancer Cells

  • Park, Deokbae;Lee, Youngki
    • 한국발생생물학회지:발생과생식
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    • 제18권4호
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    • pp.225-231
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    • 2014
  • Autophagy is a homeostatic degradation process that is involved in tumor development and normal development. Autophagy is induced in cancer cells in response to chemotherapeutic agents, and inhibition of autophagy results in enhanced cancer cell death or survival. Chloroquine (CQ), an anti-malarial drug, is a lysosomotropic agent and is currently used as a potential anticancer agent as well as an autophagy inhibitor. Here, we evaluate the characteristics of these dual activities of CQ using human colorectal cancer cell line HCT15. The results show that CQ inhibited cell viability in dose- and time-dependent manner in the range between 20 to 80 uM, while CQ did not show any antiproliferative activity at 5 and 10 uM. Cotreatment of CQ with antitumor agent NVP-BEZ235, a dual inhibitor of PI3K/mTOR, rescued the cell viability at low concentrations meaning that CQ acted as an autophagy inhibitor, but CQ induced the lethal effect at high concentrations. Acridine orange staining revealed that CQ at high doses induced lysosomal membrane permeabilization (LMP). High doses of CQ produced cellular reactive oxygen species (ROS) and cotreatment of antioxidants, such as NAC and trolox, with high doses of CQ rescued the cell viability. These results suggest that CQ may exert its dual activities, as autophagy inhibitor or LMP inducer, in concentration-dependent manner.