Proteomic Investigation to Identify Anticancer Targets of Nemopilema nomurai Jellyfish Venom in Human Hepatocarcinoma HepG2 Cells SCIE SCOPUS

DC Field Value Language
dc.contributor.author Choudhary, Indu -
dc.contributor.author Lee, Hyunkyoung -
dc.contributor.author Pyo, Min Jung -
dc.contributor.author Heo, Yunwi -
dc.contributor.author Chae, Jinho -
dc.contributor.author Yum, Seung Shic -
dc.contributor.author Kang, Changkeun -
dc.contributor.author Kim, Euikyung -
dc.date.accessioned 2020-04-16T08:55:14Z -
dc.date.available 2020-04-16T08:55:14Z -
dc.date.created 2020-01-28 -
dc.date.issued 2018-05 -
dc.identifier.issn 2072-6651 -
dc.identifier.uri https://sciwatch.kiost.ac.kr/handle/2020.kiost/915 -
dc.description.abstract Nemopilema nomurai is a giant jellyfish that blooms in East Asian seas. Recently, N. nomurai venom (NnV) was characterized from a toxicological and pharmacological point of view. A mild dose of NnV inhibits the growth of various kinds of cancer cells, mainly hepatic cancer cells. The present study aims to identify the potential therapeutic targets and mechanism of NnV in the growth inhibition of cancer cells. Human hepatocellular carcinoma (HepG2) cells were treated with NnV, and its proteome was analyzed using two-dimensional gel electrophoresis, followed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI/TOF/MS). The quantity of twenty four proteins in NnV-treated HepG2 cells varied compared to non-treated control cells. Among them, the amounts of fourteen proteins decreased and ten proteins showed elevated levels. We also found that the amounts of several cancer biomarkers and oncoproteins, which usually increase in various types of cancer cells, decreased after NnV treatment. The representative proteins included proliferating cell nuclear antigen (PCNA), glucose-regulated protein 78 (GRP78), glucose-6-phosphate dehydrogenase (G6PD), elongation factor 1 (EF1), nucleolar and spindle-associated protein (NuSAP), and activator of 90 kDa heat shock protein ATPase homolog 1 (AHSA1). Western blotting also confirmed altered levels of PCNA, GRP78, and G6PD in NnV-treated HepG2 cells. In summary, the proteomic approach explains the mode of action of NnV as an anticancer agent. Further characterization of NnV may help to unveil novel therapeutic agents in cancer treatment. -
dc.description.uri 1 -
dc.language English -
dc.publisher MDPI -
dc.subject MESSENGER-RNA EXPRESSION -
dc.subject KAPPA-B PATHWAY -
dc.subject CANCER-CELLS -
dc.subject HEPATOCELLULAR-CARCINOMA -
dc.subject GENE-EXPRESSION -
dc.subject GLUCOSE-6-PHOSPHATE-DEHYDROGENASE EXPRESSION -
dc.subject ESOPHAGEAL-CARCINOMA -
dc.subject PANCREATIC-CANCER -
dc.subject GASTRIC-CARCINOMA -
dc.subject POOR-PROGNOSIS -
dc.title Proteomic Investigation to Identify Anticancer Targets of Nemopilema nomurai Jellyfish Venom in Human Hepatocarcinoma HepG2 Cells -
dc.type Article -
dc.citation.title TOXINS -
dc.citation.volume 10 -
dc.citation.number 5 -
dc.contributor.alternativeName 염승식 -
dc.identifier.bibliographicCitation TOXINS, v.10, no.5 -
dc.identifier.doi 10.3390/toxins10050194 -
dc.identifier.scopusid 2-s2.0-85047371907 -
dc.identifier.wosid 000435198800025 -
dc.type.docType Article -
dc.description.journalClass 1 -
dc.subject.keywordPlus MESSENGER-RNA EXPRESSION -
dc.subject.keywordPlus KAPPA-B PATHWAY -
dc.subject.keywordPlus CANCER-CELLS -
dc.subject.keywordPlus HEPATOCELLULAR-CARCINOMA -
dc.subject.keywordPlus GENE-EXPRESSION -
dc.subject.keywordPlus GLUCOSE-6-PHOSPHATE-DEHYDROGENASE EXPRESSION -
dc.subject.keywordPlus ESOPHAGEAL-CARCINOMA -
dc.subject.keywordPlus PANCREATIC-CANCER -
dc.subject.keywordPlus GASTRIC-CARCINOMA -
dc.subject.keywordPlus POOR-PROGNOSIS -
dc.subject.keywordAuthor jellyfish -
dc.subject.keywordAuthor Nemopilema nomurai -
dc.subject.keywordAuthor HepG2 cell -
dc.subject.keywordAuthor venom -
dc.subject.keywordAuthor proteomics -
dc.subject.keywordAuthor MALDI/TOF/MS -
dc.subject.keywordAuthor 2-DE -
dc.relation.journalWebOfScienceCategory Food Science & Technology -
dc.relation.journalWebOfScienceCategory Toxicology -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Food Science & Technology -
dc.relation.journalResearchArea Toxicology -
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