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Identification of compounds with preferential inhibitory activity against low-Nm23-expressing human breast carcinoma and melanoma cell lines
by
Grever, Michael
, Hollingshead, Melinda G.
, De La Rosa, Abel
, Lawrence, Julia A.
, Paull, Kenneth
, Narayanan, Ven
, Sausville, Edward A.
, Steeg, Patricia S.
, Freije, José M.P.
in
Algorithms
/ Antineoplastic Agents - therapeutic use
/ Biomarkers, Tumor - analysis
/ Biomedical and Life Sciences
/ Biomedicine
/ Breast Neoplasms - drug therapy
/ Cancer Research
/ Female
/ Humans
/ Infectious Diseases
/ Melanoma - drug therapy
/ Metabolic Diseases
/ Molecular Medicine
/ Monomeric GTP-Binding Proteins
/ Neoplasm Metastasis
/ Neurosciences
/ NM23 Nucleoside Diphosphate Kinases
/ Nucleoside-Diphosphate Kinase
/ Transcription Factors - analysis
/ Tumor Cells, Cultured
1997
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Identification of compounds with preferential inhibitory activity against low-Nm23-expressing human breast carcinoma and melanoma cell lines
by
Grever, Michael
, Hollingshead, Melinda G.
, De La Rosa, Abel
, Lawrence, Julia A.
, Paull, Kenneth
, Narayanan, Ven
, Sausville, Edward A.
, Steeg, Patricia S.
, Freije, José M.P.
in
Algorithms
/ Antineoplastic Agents - therapeutic use
/ Biomarkers, Tumor - analysis
/ Biomedical and Life Sciences
/ Biomedicine
/ Breast Neoplasms - drug therapy
/ Cancer Research
/ Female
/ Humans
/ Infectious Diseases
/ Melanoma - drug therapy
/ Metabolic Diseases
/ Molecular Medicine
/ Monomeric GTP-Binding Proteins
/ Neoplasm Metastasis
/ Neurosciences
/ NM23 Nucleoside Diphosphate Kinases
/ Nucleoside-Diphosphate Kinase
/ Transcription Factors - analysis
/ Tumor Cells, Cultured
1997
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Identification of compounds with preferential inhibitory activity against low-Nm23-expressing human breast carcinoma and melanoma cell lines
by
Grever, Michael
, Hollingshead, Melinda G.
, De La Rosa, Abel
, Lawrence, Julia A.
, Paull, Kenneth
, Narayanan, Ven
, Sausville, Edward A.
, Steeg, Patricia S.
, Freije, José M.P.
in
Algorithms
/ Antineoplastic Agents - therapeutic use
/ Biomarkers, Tumor - analysis
/ Biomedical and Life Sciences
/ Biomedicine
/ Breast Neoplasms - drug therapy
/ Cancer Research
/ Female
/ Humans
/ Infectious Diseases
/ Melanoma - drug therapy
/ Metabolic Diseases
/ Molecular Medicine
/ Monomeric GTP-Binding Proteins
/ Neoplasm Metastasis
/ Neurosciences
/ NM23 Nucleoside Diphosphate Kinases
/ Nucleoside-Diphosphate Kinase
/ Transcription Factors - analysis
/ Tumor Cells, Cultured
1997
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Identification of compounds with preferential inhibitory activity against low-Nm23-expressing human breast carcinoma and melanoma cell lines
Journal Article
Identification of compounds with preferential inhibitory activity against low-Nm23-expressing human breast carcinoma and melanoma cell lines
1997
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Overview
We have used the COMPARE computer algorithm and Nm23 expression as a marker of tumor metastatic potential to examine the
in vitro
antiproliferative activity of chemotherapeutic drugs on human breast carcinoma and melanoma cell lines. None of 171 compounds in clinical use or under development and only 40 of 30,000 repository compounds exhibited preferential growth inhibition of low-Nm23-expressing, metastatically aggressive cell lines with a Pearson correlation coefficient of ≤0.64. Characterization of one compound, NSC 645306, is presented including
in vivo
activity in a hollow fiber assay. The data demonstrate a novel approach to drug identification for aggressive human tumors.
Publisher
Nature Publishing Group US
Subject
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