Nanoparticle‐biomolecular corona: A new approach for the early detection of non‐small‐cell lung cancer
Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. Non‐small‐cell lung cancer (NSCLC) is the most frequent type of LC occurring in 85% of cases. Developing new methods for early detection of NSCLC could substanti...
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Published in | Journal of cellular physiology Vol. 234; no. 6; pp. 9378 - 9386 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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01.06.2019
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Abstract | Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. Non‐small‐cell lung cancer (NSCLC) is the most frequent type of LC occurring in 85% of cases. Developing new methods for early detection of NSCLC could substantially increase the chances of survival and, therefore, is an urgent task for current research. Nowadays, explosion in nanotechnology offers unprecedented opportunities for therapeutics and diagnosis applications. In this context, exploiting the bio‐nano‐interactions between nanoparticles (NPs) and biological fluids is an emerging field of research. Upon contact with biofluids, NPs are covered by a biomolecular coating referred to as “biomolecular corona” (BC). In this study, we exploited BC for discriminating between NSCLC patients and healthy volunteers. Blood samples from 10 NSCLC patients and 5 subjects without malignancy were allowed to interact with negatively charged lipid NPs, leading to the formation of a BC at the NP surface. After isolation, BCs were characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS‐PAGE). We found that the BCs of NSCLC patients was significantly different from that of healthy individuals. Statistical analysis of SDS‐PAGE results allowed discriminating between NSCLC cancer patients and healthy subjects with 80% specificity, 80% sensitivity and a total discriminate correctness rate of 80%. While the results of the present investigation cannot be conclusive due to the small size of the data set, we have shown that exploitation of the BC is a promising approach for the early diagnosis of NSCLC.
Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. In this study, we compared biomolecular corona formed around liposomes for discriminating between NSCLC patients and healthy volunteers. Our results allowed discriminating between NSCLC cancer patients and healthy subjects with 80% specificity, 80% sensitivity, and a total discriminate correctness rate of 80%. |
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AbstractList | Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. Non‐small‐cell lung cancer (NSCLC) is the most frequent type of LC occurring in 85% of cases. Developing new methods for early detection of NSCLC could substantially increase the chances of survival and, therefore, is an urgent task for current research. Nowadays, explosion in nanotechnology offers unprecedented opportunities for therapeutics and diagnosis applications. In this context, exploiting the bio‐nano‐interactions between nanoparticles (NPs) and biological fluids is an emerging field of research. Upon contact with biofluids, NPs are covered by a biomolecular coating referred to as “biomolecular corona” (BC). In this study, we exploited BC for discriminating between NSCLC patients and healthy volunteers. Blood samples from 10 NSCLC patients and 5 subjects without malignancy were allowed to interact with negatively charged lipid NPs, leading to the formation of a BC at the NP surface. After isolation, BCs were characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS‐PAGE). We found that the BCs of NSCLC patients was significantly different from that of healthy individuals. Statistical analysis of SDS‐PAGE results allowed discriminating between NSCLC cancer patients and healthy subjects with 80% specificity, 80% sensitivity and a total discriminate correctness rate of 80%. While the results of the present investigation cannot be conclusive due to the small size of the data set, we have shown that exploitation of the BC is a promising approach for the early diagnosis of NSCLC. Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. Non‐small‐cell lung cancer (NSCLC) is the most frequent type of LC occurring in 85% of cases. Developing new methods for early detection of NSCLC could substantially increase the chances of survival and, therefore, is an urgent task for current research. Nowadays, explosion in nanotechnology offers unprecedented opportunities for therapeutics and diagnosis applications. In this context, exploiting the bio‐nano‐interactions between nanoparticles (NPs) and biological fluids is an emerging field of research. Upon contact with biofluids, NPs are covered by a biomolecular coating referred to as “biomolecular corona” (BC). In this study, we exploited BC for discriminating between NSCLC patients and healthy volunteers. Blood samples from 10 NSCLC patients and 5 subjects without malignancy were allowed to interact with negatively charged lipid NPs, leading to the formation of a BC at the NP surface. After isolation, BCs were characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS‐PAGE). We found that the BCs of NSCLC patients was significantly different from that of healthy individuals. Statistical analysis of SDS‐PAGE results allowed discriminating between NSCLC cancer patients and healthy subjects with 80% specificity, 80% sensitivity and a total discriminate correctness rate of 80%. While the results of the present investigation cannot be conclusive due to the small size of the data set, we have shown that exploitation of the BC is a promising approach for the early diagnosis of NSCLC. Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. Non‐small‐cell lung cancer (NSCLC) is the most frequent type of LC occurring in 85% of cases. Developing new methods for early detection of NSCLC could substantially increase the chances of survival and, therefore, is an urgent task for current research. Nowadays, explosion in nanotechnology offers unprecedented opportunities for therapeutics and diagnosis applications. In this context, exploiting the bio‐nano‐interactions between nanoparticles (NPs) and biological fluids is an emerging field of research. Upon contact with biofluids, NPs are covered by a biomolecular coating referred to as “biomolecular corona” (BC). In this study, we exploited BC for discriminating between NSCLC patients and healthy volunteers. Blood samples from 10 NSCLC patients and 5 subjects without malignancy were allowed to interact with negatively charged lipid NPs, leading to the formation of a BC at the NP surface. After isolation, BCs were characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS‐PAGE). We found that the BCs of NSCLC patients was significantly different from that of healthy individuals. Statistical analysis of SDS‐PAGE results allowed discriminating between NSCLC cancer patients and healthy subjects with 80% specificity, 80% sensitivity and a total discriminate correctness rate of 80%. While the results of the present investigation cannot be conclusive due to the small size of the data set, we have shown that exploitation of the BC is a promising approach for the early diagnosis of NSCLC. Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. In this study, we compared biomolecular corona formed around liposomes for discriminating between NSCLC patients and healthy volunteers. Our results allowed discriminating between NSCLC cancer patients and healthy subjects with 80% specificity, 80% sensitivity, and a total discriminate correctness rate of 80%. Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. Non-small-cell lung cancer (NSCLC) is the most frequent type of LC occurring in 85% of cases. Developing new methods for early detection of NSCLC could substantially increase the chances of survival and, therefore, is an urgent task for current research. Nowadays, explosion in nanotechnology offers unprecedented opportunities for therapeutics and diagnosis applications. In this context, exploiting the bio-nano-interactions between nanoparticles (NPs) and biological fluids is an emerging field of research. Upon contact with biofluids, NPs are covered by a biomolecular coating referred to as "biomolecular corona" (BC). In this study, we exploited BC for discriminating between NSCLC patients and healthy volunteers. Blood samples from 10 NSCLC patients and 5 subjects without malignancy were allowed to interact with negatively charged lipid NPs, leading to the formation of a BC at the NP surface. After isolation, BCs were characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). We found that the BCs of NSCLC patients was significantly different from that of healthy individuals. Statistical analysis of SDS-PAGE results allowed discriminating between NSCLC cancer patients and healthy subjects with 80% specificity, 80% sensitivity and a total discriminate correctness rate of 80%. While the results of the present investigation cannot be conclusive due to the small size of the data set, we have shown that exploitation of the BC is a promising approach for the early diagnosis of NSCLC.Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. Non-small-cell lung cancer (NSCLC) is the most frequent type of LC occurring in 85% of cases. Developing new methods for early detection of NSCLC could substantially increase the chances of survival and, therefore, is an urgent task for current research. Nowadays, explosion in nanotechnology offers unprecedented opportunities for therapeutics and diagnosis applications. In this context, exploiting the bio-nano-interactions between nanoparticles (NPs) and biological fluids is an emerging field of research. Upon contact with biofluids, NPs are covered by a biomolecular coating referred to as "biomolecular corona" (BC). In this study, we exploited BC for discriminating between NSCLC patients and healthy volunteers. Blood samples from 10 NSCLC patients and 5 subjects without malignancy were allowed to interact with negatively charged lipid NPs, leading to the formation of a BC at the NP surface. After isolation, BCs were characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). We found that the BCs of NSCLC patients was significantly different from that of healthy individuals. Statistical analysis of SDS-PAGE results allowed discriminating between NSCLC cancer patients and healthy subjects with 80% specificity, 80% sensitivity and a total discriminate correctness rate of 80%. While the results of the present investigation cannot be conclusive due to the small size of the data set, we have shown that exploitation of the BC is a promising approach for the early diagnosis of NSCLC. |
Author | Di Domenico, Marina Mahmoudi, Morteza Giordano, Antonio Caracciolo, Giulio Iorio, Rosamaria Frati, Luigi Di Carlo, Angelina Pierdiluca, Matteo Palchetti, Sara Digiacomo, Luca Astarita, Carlo Barbarino, Marcella Pozzi, Daniela Fiorelli, Alfonso Santini, Mario |
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Cites_doi | 10.2147/IJN.S109059 10.1021/nn305337c 10.18632/oncotarget.16300 10.1016/j.biocel.2016.03.016 10.1039/C5NR00520E 10.4238/gmr.15027955 10.1093/icvts/ivv378 10.1016/j.bbamem.2015.11.012 10.4065/83.3.355 10.1021/ja107583h 10.1021/la401192x 10.1039/C4RA13335H 10.1039/C5NR03701H 10.1039/C1CS15233E 10.1039/C6NR05609A 10.1021/ja2084338 10.1038/nrclinonc.2016.203 10.1021/am404171h 10.1039/C4TB01316F 10.1038/nnano.2013.181 10.2217/nnm.15.188 10.1016/j.athoracsur.2014.11.049 10.1200/jco.2006.24.18_suppl.7082 10.1021/la202912f 10.5966/sctm.2015-0374 10.1016/S0025-6196(11)60735-0 10.1039/C6RA25493D 10.1039/C4BM00131A 10.1016/j.nantod.2016.10.005 10.1021/mp400470p 10.1371/journal.pone.0135331 10.18632/oncoscience.163 10.1021/nn201950e 10.1021/acsami.5b00371 |
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References | e_1_2_6_1_7_1 e_1_2_6_1_30_1 e_1_2_6_1_6_1 e_1_2_6_1_9_1 e_1_2_6_1_8_1 e_1_2_6_1_3_1 e_1_2_6_1_11_1 e_1_2_6_1_34_1 e_1_2_6_1_2_1 e_1_2_6_1_12_1 e_1_2_6_1_33_1 e_1_2_6_1_5_1 e_1_2_6_1_32_1 e_1_2_6_1_4_1 e_1_2_6_1_10_1 e_1_2_6_1_31_1 e_1_2_6_1_27_1 e_1_2_6_1_26_1 e_1_2_6_1_25_1 e_1_2_6_1_24_1 e_1_2_6_1_29_1 e_1_2_6_1_28_1 e_1_2_6_1_23_1 e_1_2_6_1_22_1 e_1_2_6_1_21_1 e_1_2_6_1_20_1 e_1_2_6_1_15_1 e_1_2_6_1_16_1 e_1_2_6_1_13_1 e_1_2_6_1_36_1 e_1_2_6_1_14_1 e_1_2_6_1_35_1 e_1_2_6_1_19_1 e_1_2_6_1_17_1 e_1_2_6_1_18_1 |
References_xml | – ident: e_1_2_6_1_11_1 doi: 10.2147/IJN.S109059 – ident: e_1_2_6_1_20_1 doi: 10.1021/nn305337c – ident: e_1_2_6_1_12_1 doi: 10.18632/oncotarget.16300 – ident: e_1_2_6_1_19_1 doi: 10.1016/j.biocel.2016.03.016 – ident: e_1_2_6_1_17_1 doi: 10.1039/C5NR00520E – ident: e_1_2_6_1_30_1 doi: 10.4238/gmr.15027955 – ident: e_1_2_6_1_14_1 doi: 10.1093/icvts/ivv378 – ident: e_1_2_6_1_25_1 doi: 10.1016/j.bbamem.2015.11.012 – ident: e_1_2_6_1_31_1 doi: 10.4065/83.3.355 – ident: e_1_2_6_1_23_1 doi: 10.1021/ja107583h – ident: e_1_2_6_1_3_1 doi: 10.1021/la401192x – ident: e_1_2_6_1_7_1 doi: 10.1039/C4RA13335H – ident: e_1_2_6_1_26_1 doi: 10.1039/C5NR03701H – ident: e_1_2_6_1_34_1 doi: 10.1039/C1CS15233E – ident: e_1_2_6_1_4_1 doi: 10.1039/C6NR05609A – ident: e_1_2_6_1_35_1 doi: 10.1021/ja2084338 – ident: e_1_2_6_1_29_1 doi: 10.1038/nrclinonc.2016.203 – ident: e_1_2_6_1_5_1 doi: 10.1021/am404171h – ident: e_1_2_6_1_8_1 doi: 10.1039/C4TB01316F – ident: e_1_2_6_1_32_1 doi: 10.1038/nnano.2013.181 – ident: e_1_2_6_1_10_1 doi: 10.2217/nnm.15.188 – ident: e_1_2_6_1_13_1 doi: 10.1016/j.athoracsur.2014.11.049 – ident: e_1_2_6_1_24_1 doi: 10.1200/jco.2006.24.18_suppl.7082 – ident: e_1_2_6_1_6_1 doi: 10.1021/la202912f – ident: e_1_2_6_1_9_1 doi: 10.5966/sctm.2015-0374 – ident: e_1_2_6_1_22_1 doi: 10.1016/S0025-6196(11)60735-0 – ident: e_1_2_6_1_2_1 doi: 10.1039/C6RA25493D – ident: e_1_2_6_1_16_1 doi: 10.1039/C4BM00131A – ident: e_1_2_6_1_21_1 doi: 10.1016/j.nantod.2016.10.005 – ident: e_1_2_6_1_15_1 – ident: e_1_2_6_1_27_1 doi: 10.1021/mp400470p – ident: e_1_2_6_1_18_1 doi: 10.1371/journal.pone.0135331 – ident: e_1_2_6_1_28_1 doi: 10.18632/oncoscience.163 – ident: e_1_2_6_1_33_1 doi: 10.1021/nn201950e – ident: e_1_2_6_1_36_1 doi: 10.1021/acsami.5b00371 |
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Snippet | Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. Non‐small‐cell lung... Lung cancer (LC) is the most common type of cancer and the second cause of death worldwide in men and women after cardiovascular diseases. Non-small-cell lung... |
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SubjectTerms | biomolecular corona Blood Proteins - metabolism Cancer Carcinoma, Non-Small-Cell Lung - blood Carcinoma, Non-Small-Cell Lung - diagnosis Cardiovascular diseases Diagnosis Dynamic Light Scattering Early Detection of Cancer Electrophoresis Gel electrophoresis Heart diseases Humans Hydrodynamics Lipids Liposomes - chemistry Lung cancer Lung diseases Lung Neoplasms - blood Lung Neoplasms - diagnosis Malignancy nanoparticle Nanoparticles Nanoparticles - chemistry Nanotechnology Non-small cell lung carcinoma non‐small‐cell lung cancer Patients Principal Component Analysis Sodium dodecyl sulfate Sodium lauryl sulfate Statistical analysis Statistical methods |
Title | Nanoparticle‐biomolecular corona: A new approach for the early detection of non‐small‐cell lung cancer |
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