Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología

Autores:: Reyna Villasmil, Eduardo

Tipo de recurso:: Article of journal

Fecha de publicación:: 2020

Institución:: Fundación Universitaria de Ciencias de la Salud - FUCS

Repositorio:: Repositorio Digital Institucional ReDi

Idioma:: spa

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dc.title.spa.fl_str_mv	Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología
dc.title.translated.eng.fl_str_mv	Usefulness of precision medicine in improving prevention, treatment and prognosis in oncology
title	Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología
spellingShingle	Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología Oncología Medicina de precisión Prevención Diagnóstico Tratamiento. Medicina Medicina de precisión Oncology Precision medicine Prevention Diagnosis Treatment
title_short	Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología
title_full	Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología
title_fullStr	Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología
title_full_unstemmed	Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología
title_sort	Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología
dc.creator.fl_str_mv	Reyna Villasmil, Eduardo
dc.contributor.author.spa.fl_str_mv	Reyna Villasmil, Eduardo
dc.subject.spa.fl_str_mv	Oncología Medicina de precisión Prevención Diagnóstico Tratamiento. Medicina Medicina de precisión
topic	Oncología Medicina de precisión Prevención Diagnóstico Tratamiento. Medicina Medicina de precisión Oncology Precision medicine Prevention Diagnosis Treatment
dc.subject.eng.fl_str_mv	Oncology Precision medicine Prevention Diagnosis Treatment
publishDate	2020
dc.date.accessioned.none.fl_str_mv	2020-04-06 16:33:03 2022-06-29T19:39:36Z
dc.date.issued.none.fl_str_mv	2020-04-06
dc.date.available.none.fl_str_mv	2020-04-06 16:33:03 2022-06-29T19:39:36Z
dc.type.spa.fl_str_mv	Artículo de revista
dc.type.eng.fl_str_mv	Journal article
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dc.identifier.url.none.fl_str_mv	https://revistas.fucsalud.edu.co/index.php/repertorio/article/view/1279
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url	https://repositorio.fucsalud.edu.co/handle/001/3083 https://revistas.fucsalud.edu.co/index.php/repertorio/article/view/1279
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dc.relation.references.spa.fl_str_mv	Santos-Cortez RLP, Bhutta MF, Earl JP, Hafrén L, Jennings M, Mell JC, Pichichero ME, Ryan AF, Tateossian H, Ehrlich GD. Panel 3: Genomics, precision medicine and targeted therapies. Int J Pediatr Otorhinolaryngol. 2020;130 Suppl 1(Suppl 1):109835. doi: 10.1016/j.ijporl.2019.109835. 2. Amekyeh H, Tarlochan F, Billa N. Practicality of 3D printed personalized medicines in therapeutics. Front Pharmacol. 2021;12:646836. doi: 10.3389/fphar.2021.646836. 3. Hebar A, Valent P, Selzer E. The impact of molecular targets in cancer drug development: major hurdles and future strategies. Expert Rev Clin Pharmacol. 2013;6(1):23-34. doi: 10.1586/ecp.12.71. 4. Yu Z, Song M, Chouchane L, Ma X. Functional genomic analysis of breast cancer metastasis: implications for diagnosis and therapy. Cancers (Basel). 2021;13(13):3276. doi: 10.3390/cancers13133276. 5. Huebner T, Scholl C, Steffens M. Cytogenetic and biochemical genetic techniques for personalized drug therapy in Europe. Diagnostics (Basel). 2021;11(7):1169. doi: 10.3390/diagnostics11071169. 6. Norrie JL, Nityanandam A, Lai K, Chen X, Wilson M, Stewart E, Griffiths L, Jin H, Wu G, Orr B, Tran Q, Allen S, Reilly C, Zhou X, Zhang J, Newman K, Johnson D, Brennan R, Dyer MA. Retinoblastoma from human stem cell-derived retinal organoids. Nat Commun. 2021;12(1):4535. doi: 10.1038/s41467-021-24781-7. 7. Heck JE, Huang X, Calkins KL, Sun Y, Olsen J, Ritz B, Hansen J. Phototherapy and childhood cancer: Shared risk factors. Int J Cancer. 2020;146(7):2059-2062. doi: 10.1002/ijc.32701. 8. Houlston R. Identification of low-penetrance alleles associated with colon cancer risk. Med Sci (Paris). 2009;25 Spec No 1:39-41. doi: 10.1051/medsci/2009251s39. 9. Capellini A, Williams M, Onel K, Huang KL. The functional hallmarks of cancer predisposition genes. Cancer Manag Res. 2021;13:4351-4357. doi: 10.2147/CMAR.S311548. 10. Bharucha PP, Chiu KE, François FM, Scott JL, Khorjekar GR, Tirada NP. Genetic testing and screening recommendations for patients with hereditary breast cancer. Radiographics. 2020;40(4):913-936. doi: 10.1148/rg.2020190181. 11. Howard TP, Vazquez F, Tsherniak A, Hong AL, Rinne M, Aguirre AJ, Boehm JS, Hahn WC. Functional genomic characterization of cancer genomes. Cold Spring Harb Symp Quant Biol. 2016;81:237-246. doi: 10.1101/sqb.2016.81.031070. 12. Kutkowska J, Strzadala L, Rapak A. Synergistic activity of sorafenib and betulinic acid against clonogenic activity of non-small cell lung cancer cells. Cancer Sci. 2017;108(11):2265-2272. doi: 10.1111/cas.13386. 13. Chen L, Liu S, Tao Y. Regulating tumor suppressor genes: post-translational modifications. Signal Transduct Target Ther. 2020;5(1):90. doi: 10.1038/s41392-020-0196-9. 14. Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646-74. doi: 10.1016/j.cell.2011.02.013. 15. Gisselsson D, Egnell R. Cancer - An insurgency of clones. Trends Cancer. 2017;3(2):73-75. doi: 10.1016/j.trecan.2016.11.010. 16. Soltanian S, Matin MM. Cancer stem cells and cancer therapy. Tumour Biol. 2011;32(3):425-40. doi: 10.1007/s13277-011-0155-8. 17. Beijnen JH, Schellens JH. Personalized medicine in oncology: a personal view with myths and facts. Curr Clin Pharmacol. 2010;5(3):141-7. doi: 10.2174/157488410791498789. 18. Vishwakarma R, McManus KJ. Chromosome instability; Implications in cancer development, progression, and clinical outcomes. Cancers (Basel). 2020;12(4):824. doi: 10.3390/cancers12040824. 19. Mainor CB, Isaacs C. Risk Management for BRCA1/BRCA2 mutation carriers without and with breast cancer. Curr Breast Cancer Rep. 2020;12(2):66-74. doi: 10.1007/s12609-019-00350-2. 20. Lewis KM. Identifying hereditary cancer: genetic counseling and cancer risk assessment. Curr Probl Cancer. 2014;38(6):216-25. doi: 10.1016/j.currproblcancer.2014.10.002. 21. McClellan J, King MC. Genetic heterogeneity in human disease. Cell. 2010;141(2):210-7. doi: 10.1016/j.cell.2010.03.032. 22. Tian H, Gao Z, Li H, Zhang B, Wang G, Zhang Q, Pei D, Zheng J. DNA damage response--a double-edged sword in cancer prevention and cancer therapy. Cancer Lett. 2015;358(1):8-16. doi: 10.1016/j.canlet.2014.12.038. 23. Szczerba E, Kamińska K, Mierzwa T, Misiek M, Kowalewski J, Lewandowska MA. BRCA1/2 mutation detection in the tumor tissue from selected polish patients with breast cancer using Next Generation Sequencing. Genes (Basel). 2021;12(4):519. doi: 10.3390/genes12040519. 24. Landrum MJ, Chitipiralla S, Brown GR, Chen C, Gu B, Hart J, Hoffman D, Jang W, Kaur K, Liu C, Lyoshin V, Maddipatla Z, Maiti R, Mitchell J, O'Leary N, Riley GR, Shi W, Zhou G, Schneider V, Maglott D, Holmes JB, Kattman BL. ClinVar: improvements to accessing data. Nucleic Acids Res. 2020;48(D1):D835-D844. doi: 10.1093/nar/gkz972. 25. Dumbrava EI, Meric-Bernstam F. Personalized cancer therapy-leveraging a knowledge base for clinical decision-making. Cold Spring Harb Mol Case Stud. 2018;4(2):a001578. doi: 10.1101/mcs.a001578. 26. Hughes E, Tshiaba P, Wagner S, Judkins T, Rosenthal E, Roa B, Gallagher S, Meek S, Dalton K, Hedegard W, Adami CA, Grear DF, Domchek SM, Garber J, Lancaster JM, Weitzel JN, Kurian AW, Lanchbury JS, Gutin A, Robson ME. Integrating clinical and polygenic factors to predict breast cancer risk in women undergoing genetic testing. JCO Precis Oncol. 2021;5:PO.20.00246. doi: 10.1200/PO.20.00246. 27. Qiu J, Xu J, Zhang K, Gu W, Nie L, Wang G, Luo Y. Refining cancer management using integrated liquid biopsy. Theranostics. 2020;10(5):2374-2384. doi: 10.7150/thno.40677. 28. Kristensen BW, Priesterbach-Ackley LP, Petersen JK, Wesseling P. Molecular pathology of tumors of the central nervous system. Ann Oncol. 2019;30(8):1265-1278. doi: 10.1093/annonc/mdz164. 29. Elkamhawy A, Lu Q, Nada H, Woo J, Quan G, Lee K. The Journey of DDR1 and DDR2 Kinase Inhibitors as Rising Stars in the Fight Against Cancer. Int J Mol Sci. 2021;22(12):6535. doi: 10.3390/ijms22126535. 30. Krzyszczyk P, Acevedo A, Davidoff EJ, Timmins LM, Marrero-Berrios I, Patel M, White C, Lowe C, Sherba JJ, Hartmanshenn C, O'Neill KM, Balter ML, Fritz ZR, Androulakis IP, Schloss RS, Yarmush ML. The growing role of precision and personalized medicine for cancer treatment. Technology (Singap World Sci). 2018;6(3-4):79-100. doi: 10.1142/S2339547818300020. 31. Helgadottir H, Rocha Trocoli Drakensjö I, Girnita A. Personalized medicine in malignant melanoma: Towards patient tailored treatment. Front Oncol. 2018;8:202. doi: 10.3389/fonc.2018.00202. 32. Afrăsânie VA, Marinca MV, Alexa-Stratulat T, Gafton B, Păduraru M, Adavidoaiei AM, Miron L, Rusu C. KRAS, NRAS, BRAF, HER2 and microsatellite instability in metastatic colorectal cancer - practical implications for the clinician. Radiol Oncol. 2019;53(3):265-274. doi: 10.2478/raon-2019-0033. 33. von Manstein V, Yang CM, Richter D, Delis N, Vafaizadeh V, Groner B. Resistance of cancer cells to targeted therapies through the activation of compensating signaling loops. Curr Signal Transduct Ther. 2013;8(3):193-202. doi: 10.2174/1574362409666140206221931. 34. Vieira AF, Schmitt F. An update on breast cancer multigene prognostic tests-emergent clinical biomarkers. Front Med (Lausanne). 2018;5:248. doi: 10.3389/fmed.2018.00248. 35. Schildgen V, Warm M, Brockmann M, Schildgen O. Oncotype DX Breast Cancer recurrence score resists inter-assay reproducibility with RT2-Profiler Multiplex RT-PCR. Sci Rep. 2019;9(1):20266. doi: 10.1038/s41598-019-56910-0.
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spelling	Reyna Villasmil, Eduardo3b512367dfc5517e0abaabf4232b69c22020-04-06 16:33:032022-06-29T19:39:36Z2020-04-062020-04-06 16:33:032022-06-29T19:39:36ZSociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la SaludRevista Repertorio de Medicina y Cirugía - 2020info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/4.0/http://purl.org/coar/access_right/c_abf2https://revistas.fucsalud.edu.co/index.php/repertorio/article/view/1279OncologíaMedicina de precisiónPrevenciónDiagnósticoTratamiento.MedicinaMedicina de precisiónOncologyPrecision medicinePreventionDiagnosisTreatmentUtilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncologíaUsefulness of precision medicine in improving prevention, treatment and prognosis in oncologyapplication/pdfArtículo de revistaJournal articlehttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_dcae04bchttp://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionTexthttp://purl.org/redcol/resource_type/ARTREVhttp://purl.org/coar/version/c_970fb48d4fbd8a850121-7372https://repositorio.fucsalud.edu.co/handle/001/30832462-991Xhttps://revistas.fucsalud.edu.co/index.php/repertorio/article/view/1279spaSantos-Cortez RLP, Bhutta MF, Earl JP, Hafrén L, Jennings M, Mell JC, Pichichero ME, Ryan AF, Tateossian H, Ehrlich GD. Panel 3: Genomics, precision medicine and targeted therapies. Int J Pediatr Otorhinolaryngol. 2020;130 Suppl 1(Suppl 1):109835. doi: 10.1016/j.ijporl.2019.109835. 2. Amekyeh H, Tarlochan F, Billa N. Practicality of 3D printed personalized medicines in therapeutics. Front Pharmacol. 2021;12:646836. doi: 10.3389/fphar.2021.646836. 3. Hebar A, Valent P, Selzer E. The impact of molecular targets in cancer drug development: major hurdles and future strategies. Expert Rev Clin Pharmacol. 2013;6(1):23-34. doi: 10.1586/ecp.12.71. 4. Yu Z, Song M, Chouchane L, Ma X. Functional genomic analysis of breast cancer metastasis: implications for diagnosis and therapy. Cancers (Basel). 2021;13(13):3276. doi: 10.3390/cancers13133276. 5. Huebner T, Scholl C, Steffens M. Cytogenetic and biochemical genetic techniques for personalized drug therapy in Europe. Diagnostics (Basel). 2021;11(7):1169. doi: 10.3390/diagnostics11071169. 6. Norrie JL, Nityanandam A, Lai K, Chen X, Wilson M, Stewart E, Griffiths L, Jin H, Wu G, Orr B, Tran Q, Allen S, Reilly C, Zhou X, Zhang J, Newman K, Johnson D, Brennan R, Dyer MA. Retinoblastoma from human stem cell-derived retinal organoids. Nat Commun. 2021;12(1):4535. doi: 10.1038/s41467-021-24781-7. 7. Heck JE, Huang X, Calkins KL, Sun Y, Olsen J, Ritz B, Hansen J. Phototherapy and childhood cancer: Shared risk factors. Int J Cancer. 2020;146(7):2059-2062. doi: 10.1002/ijc.32701. 8. Houlston R. Identification of low-penetrance alleles associated with colon cancer risk. Med Sci (Paris). 2009;25 Spec No 1:39-41. doi: 10.1051/medsci/2009251s39. 9. Capellini A, Williams M, Onel K, Huang KL. The functional hallmarks of cancer predisposition genes. Cancer Manag Res. 2021;13:4351-4357. doi: 10.2147/CMAR.S311548. 10. Bharucha PP, Chiu KE, François FM, Scott JL, Khorjekar GR, Tirada NP. Genetic testing and screening recommendations for patients with hereditary breast cancer. Radiographics. 2020;40(4):913-936. doi: 10.1148/rg.2020190181. 11. Howard TP, Vazquez F, Tsherniak A, Hong AL, Rinne M, Aguirre AJ, Boehm JS, Hahn WC. Functional genomic characterization of cancer genomes. Cold Spring Harb Symp Quant Biol. 2016;81:237-246. doi: 10.1101/sqb.2016.81.031070. 12. Kutkowska J, Strzadala L, Rapak A. Synergistic activity of sorafenib and betulinic acid against clonogenic activity of non-small cell lung cancer cells. Cancer Sci. 2017;108(11):2265-2272. doi: 10.1111/cas.13386. 13. Chen L, Liu S, Tao Y. Regulating tumor suppressor genes: post-translational modifications. Signal Transduct Target Ther. 2020;5(1):90. doi: 10.1038/s41392-020-0196-9. 14. Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646-74. doi: 10.1016/j.cell.2011.02.013. 15. Gisselsson D, Egnell R. Cancer - An insurgency of clones. Trends Cancer. 2017;3(2):73-75. doi: 10.1016/j.trecan.2016.11.010. 16. Soltanian S, Matin MM. Cancer stem cells and cancer therapy. Tumour Biol. 2011;32(3):425-40. doi: 10.1007/s13277-011-0155-8. 17. Beijnen JH, Schellens JH. Personalized medicine in oncology: a personal view with myths and facts. Curr Clin Pharmacol. 2010;5(3):141-7. doi: 10.2174/157488410791498789. 18. Vishwakarma R, McManus KJ. Chromosome instability; Implications in cancer development, progression, and clinical outcomes. Cancers (Basel). 2020;12(4):824. doi: 10.3390/cancers12040824. 19. Mainor CB, Isaacs C. Risk Management for BRCA1/BRCA2 mutation carriers without and with breast cancer. Curr Breast Cancer Rep. 2020;12(2):66-74. doi: 10.1007/s12609-019-00350-2. 20. Lewis KM. Identifying hereditary cancer: genetic counseling and cancer risk assessment. Curr Probl Cancer. 2014;38(6):216-25. doi: 10.1016/j.currproblcancer.2014.10.002. 21. McClellan J, King MC. Genetic heterogeneity in human disease. Cell. 2010;141(2):210-7. doi: 10.1016/j.cell.2010.03.032. 22. Tian H, Gao Z, Li H, Zhang B, Wang G, Zhang Q, Pei D, Zheng J. DNA damage response--a double-edged sword in cancer prevention and cancer therapy. Cancer Lett. 2015;358(1):8-16. doi: 10.1016/j.canlet.2014.12.038. 23. Szczerba E, Kamińska K, Mierzwa T, Misiek M, Kowalewski J, Lewandowska MA. BRCA1/2 mutation detection in the tumor tissue from selected polish patients with breast cancer using Next Generation Sequencing. Genes (Basel). 2021;12(4):519. doi: 10.3390/genes12040519. 24. Landrum MJ, Chitipiralla S, Brown GR, Chen C, Gu B, Hart J, Hoffman D, Jang W, Kaur K, Liu C, Lyoshin V, Maddipatla Z, Maiti R, Mitchell J, O'Leary N, Riley GR, Shi W, Zhou G, Schneider V, Maglott D, Holmes JB, Kattman BL. ClinVar: improvements to accessing data. Nucleic Acids Res. 2020;48(D1):D835-D844. doi: 10.1093/nar/gkz972. 25. Dumbrava EI, Meric-Bernstam F. Personalized cancer therapy-leveraging a knowledge base for clinical decision-making. Cold Spring Harb Mol Case Stud. 2018;4(2):a001578. doi: 10.1101/mcs.a001578. 26. Hughes E, Tshiaba P, Wagner S, Judkins T, Rosenthal E, Roa B, Gallagher S, Meek S, Dalton K, Hedegard W, Adami CA, Grear DF, Domchek SM, Garber J, Lancaster JM, Weitzel JN, Kurian AW, Lanchbury JS, Gutin A, Robson ME. Integrating clinical and polygenic factors to predict breast cancer risk in women undergoing genetic testing. JCO Precis Oncol. 2021;5:PO.20.00246. doi: 10.1200/PO.20.00246. 27. Qiu J, Xu J, Zhang K, Gu W, Nie L, Wang G, Luo Y. Refining cancer management using integrated liquid biopsy. Theranostics. 2020;10(5):2374-2384. doi: 10.7150/thno.40677. 28. Kristensen BW, Priesterbach-Ackley LP, Petersen JK, Wesseling P. Molecular pathology of tumors of the central nervous system. Ann Oncol. 2019;30(8):1265-1278. doi: 10.1093/annonc/mdz164. 29. Elkamhawy A, Lu Q, Nada H, Woo J, Quan G, Lee K. The Journey of DDR1 and DDR2 Kinase Inhibitors as Rising Stars in the Fight Against Cancer. Int J Mol Sci. 2021;22(12):6535. doi: 10.3390/ijms22126535. 30. Krzyszczyk P, Acevedo A, Davidoff EJ, Timmins LM, Marrero-Berrios I, Patel M, White C, Lowe C, Sherba JJ, Hartmanshenn C, O'Neill KM, Balter ML, Fritz ZR, Androulakis IP, Schloss RS, Yarmush ML. The growing role of precision and personalized medicine for cancer treatment. Technology (Singap World Sci). 2018;6(3-4):79-100. doi: 10.1142/S2339547818300020. 31. Helgadottir H, Rocha Trocoli Drakensjö I, Girnita A. Personalized medicine in malignant melanoma: Towards patient tailored treatment. Front Oncol. 2018;8:202. doi: 10.3389/fonc.2018.00202. 32. Afrăsânie VA, Marinca MV, Alexa-Stratulat T, Gafton B, Păduraru M, Adavidoaiei AM, Miron L, Rusu C. KRAS, NRAS, BRAF, HER2 and microsatellite instability in metastatic colorectal cancer - practical implications for the clinician. Radiol Oncol. 2019;53(3):265-274. doi: 10.2478/raon-2019-0033. 33. von Manstein V, Yang CM, Richter D, Delis N, Vafaizadeh V, Groner B. Resistance of cancer cells to targeted therapies through the activation of compensating signaling loops. Curr Signal Transduct Ther. 2013;8(3):193-202. doi: 10.2174/1574362409666140206221931. 34. Vieira AF, Schmitt F. An update on breast cancer multigene prognostic tests-emergent clinical biomarkers. Front Med (Lausanne). 2018;5:248. doi: 10.3389/fmed.2018.00248. 35. Schildgen V, Warm M, Brockmann M, Schildgen O. Oncotype DX Breast Cancer recurrence score resists inter-assay reproducibility with RT2-Profiler Multiplex RT-PCR. Sci Rep. 2019;9(1):20266. doi: 10.1038/s41598-019-56910-0.https://revistas.fucsalud.edu.co/index.php/repertorio/article/download/1279/1861: Pre-PrintRevista Repertorio de Medicina y CirugíaPublicationOREORE.xmltext/xml2681https://repositorio.fucsalud.edu.co/bitstreams/034b4c91-8d55-455d-bcb7-bf68d02ef542/downloadaf1d93828565b4ddc27c39cf590226b1MD51001/3083oai:repositorio.fucsalud.edu.co:001/30832024-02-02 13:07:14.938https://creativecommons.org/licenses/by-nc-sa/4.0/Revista Repertorio de Medicina y Cirugía - 2020metadata.onlyhttps://repositorio.fucsalud.edu.coRepositorio Digital de la Fundación Universitaria de Ciencias de la Saludredi@fucsalud.edu.co

Utilidad en la prevención, tratamiento y pronóstico de la medicina de precisión en oncología

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