mLST8 Promotes mTOR-Mediated Tumor Progression
Publication Date
April 23, 2015
Journal
PLOS ONE
Authors
Kyoko Kakumoto, Jun Ichiro Ikeda, Masato Okada, Eiichi Morii, et al
Volume
10
Issue
4
Pages
e0119015
DOI
https://dx.plos.org/10.1371/journal.pone.0119015
Publisher URL
http://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0119015
Web of Science
000353332000002
Scopus
84929359506
Mendeley
http://www.mendeley.com/research/mlst8-promotes-mtormediated-tumor-progression
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Mendeley | Further Information

{"title"=>"MLST8 promotes mTOR-mediated tumor progression", "type"=>"journal", "authors"=>[{"first_name"=>"Kyoko", "last_name"=>"Kakumoto", "scopus_author_id"=>"8714209300"}, {"first_name"=>"Jun Ichiro", "last_name"=>"Ikeda", "scopus_author_id"=>"16746852900"}, {"first_name"=>"Masato", "last_name"=>"Okada", "scopus_author_id"=>"35300403700"}, {"first_name"=>"Eiichi", "last_name"=>"Morii", "scopus_author_id"=>"7003914326"}, {"first_name"=>"Chitose", "last_name"=>"Oneyama", "scopus_author_id"=>"6506459166"}], "year"=>2015, "source"=>"PLoS ONE", "identifiers"=>{"scopus"=>"2-s2.0-84929359506", "sgr"=>"84929359506", "issn"=>"19326203", "doi"=>"10.1371/journal.pone.0119015", "pmid"=>"25906254", "isbn"=>"10.1371/journal.pone.0119015", "pui"=>"604371900"}, "id"=>"fbc587d3-3eb6-36a8-922d-199f2b821600", "abstract"=>"The activity of the mechanistic target of rapamycin (mTOR) is elevated in various types of human cancers, implicating a role in tumor progression. However, the molecular mechanisms underlying mTOR upregulation remain unclear. In this study, we found that the expression of mLST8, a required subunit of both mTOR complex 1 (mTORC1) and complex 2 (mTORC2), was upregulated in several human colon and prostate cancer cell lines and tissues. Knockdown of mLST8 significantly suppressed mTORC1 and mTORC2 complex formation, and it also inhibited tumor growth and invasiveness in human colon carcinoma (HCT116) and prostate cancer (LNCaP) cells. Overexpression of mLST8 induced anchorage-independent cell growth in normal epithelial cells (HaCaT), although mLST8 knockdown had no effect on normal cell growth. mLST8 knockdown reduced mTORC2-mediated phosphorylation of AKT in both cancer and normal cells, whereas it potently inhibited mTORC1-mediated phosphorylation of 4E-BP1 specifically in cancer cells. These results suggest that mLST8 plays distinct roles in normal and cancer cells, depending upon its expression level, and that mLST8 upregulation may contribute to tumor progression by constitutively activating both the mTORC1 and mTORC2 pathways.", "link"=>"http://www.mendeley.com/research/mlst8-promotes-mtormediated-tumor-progression", "reader_count"=>17, "reader_count_by_academic_status"=>{"Researcher"=>3, "Student > Doctoral Student"=>2, "Student > Ph. D. Student"=>1, "Other"=>2, "Student > Master"=>2, "Student > Bachelor"=>5, "Professor"=>2}, "reader_count_by_user_role"=>{"Researcher"=>3, "Student > Doctoral Student"=>2, "Student > Ph. D. Student"=>1, "Other"=>2, "Student > Master"=>2, "Student > Bachelor"=>5, "Professor"=>2}, "reader_count_by_subject_area"=>{"Biochemistry, Genetics and Molecular Biology"=>10, "Medicine and Dentistry"=>2, "Agricultural and Biological Sciences"=>4, "Physics and Astronomy"=>1}, "reader_count_by_subdiscipline"=>{"Medicine and Dentistry"=>{"Medicine and Dentistry"=>2}, "Physics and Astronomy"=>{"Physics and Astronomy"=>1}, "Agricultural and Biological Sciences"=>{"Agricultural and Biological Sciences"=>4}, "Biochemistry, Genetics and Molecular Biology"=>{"Biochemistry, Genetics and Molecular Biology"=>10}}, "group_count"=>0}

Scopus | Further Information

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