DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutations
- Autores
- Abba, Martín Carlos; Zhong, Yi; Lee, Jaeho; Kil, Hyunsuk; Lu, Yue; Takata, Yoko; Simper, Melissa S.; Gaddis, Sally; Shen, Jianjun; Aldaz, C. Marcelo
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Controversy always existed on the utility of chemically induced mouse mammary carcinogenesis models as valid equivalents for the study of human breast cancer. Here, we performed whole exome and RNA sequencing on long latency mammary tumors (218 ± 27 days) induced by the carcinogen 7,12-Dimethylbenzathracene (DMBA) and short latency tumors (65 ± 11 days) induced by the progestin Medroxyprogesterone Acetate (MPA) plus DMBA in CD2F1 mice. Long latency tumors displayed a high frequency of Pi3kca and/or Pten mutations detected in 11 of 13 (85%) long latency cases (14/22, 64% overall). Eighty-two percent (9/11) of tumors carried the Pik3ca H1047L/R hotspot mutation, as frequently found in human breast cancer. These tumors were luminallike and mostly ER/PR+, as in humans. Transcriptome profiling indicated a significant activation of the PI3K-Akt pathway (p=3.82e-6). On the other hand MPA+DMBA induced short latency tumors displayed mutations in cancer drivers not commonly found mutated in human breast cancer (e.g. Hras and Apc). These tumors were mostly basal-like and MPA exposure led to Rankl overexpression (60 fold induction) and immunosuppressive gene expression signatures. In summary, long latency DMBA induced mouse mammary tumors reproduce the molecular profile of human luminal breast carcinomas representing an excellent preclinical model for the testing of PIK3CA/Akt/mTOR pathway inhibitory therapies and a good platform for the developing of additional preclinical tools such as syngeneic transplants in immunocompetent hosts.
Facultad de Ciencias Médicas
Centro de Investigaciones Inmunológicas Básicas y Aplicadas - Materia
-
Ciencias Médicas
DMBA
Mammary tumors
MPA
Pik3ca
Pten - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/3.0/
- Repositorio
.jpg)
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/86650
Ver los metadatos del registro completo
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DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutationsAbba, Martín CarlosZhong, YiLee, JaehoKil, HyunsukLu, YueTakata, YokoSimper, Melissa S.Gaddis, SallyShen, JianjunAldaz, C. MarceloCiencias MédicasDMBAMammary tumorsMPAPik3caPtenControversy always existed on the utility of chemically induced mouse mammary carcinogenesis models as valid equivalents for the study of human breast cancer. Here, we performed whole exome and RNA sequencing on long latency mammary tumors (218 ± 27 days) induced by the carcinogen 7,12-Dimethylbenzathracene (DMBA) and short latency tumors (65 ± 11 days) induced by the progestin Medroxyprogesterone Acetate (MPA) plus DMBA in CD2F1 mice. Long latency tumors displayed a high frequency of <i>Pi3kca</i> and/or <i>Pten</i> mutations detected in 11 of 13 (85%) long latency cases (14/22, 64% overall). Eighty-two percent (9/11) of tumors carried the <i>Pik3ca</i> H1047L/R hotspot mutation, as frequently found in human breast cancer. These tumors were luminallike and mostly ER/PR+, as in humans. Transcriptome profiling indicated a significant activation of the PI3K-Akt pathway (p=3.82e-6). On the other hand MPA+DMBA induced short latency tumors displayed mutations in cancer drivers not commonly found mutated in human breast cancer (e.g. <i>Hras</i> and <i>Apc</i>). These tumors were mostly basal-like and MPA exposure led to <i>Rankl</i> overexpression (60 fold induction) and immunosuppressive gene expression signatures. In summary, long latency DMBA induced mouse mammary tumors reproduce the molecular profile of human luminal breast carcinomas representing an excellent preclinical model for the testing of PIK3CA/Akt/mTOR pathway inhibitory therapies and a good platform for the developing of additional preclinical tools such as syngeneic transplants in immunocompetent hosts.Facultad de Ciencias MédicasCentro de Investigaciones Inmunológicas Básicas y Aplicadas2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf64289-64299http://sedici.unlp.edu.ar/handle/10915/86650enginfo:eu-repo/semantics/altIdentifier/issn/1949-2553info:eu-repo/semantics/altIdentifier/doi/10.18632/oncotarget.11733info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/3.0/Creative Commons Attribution 3.0 Unported (CC BY 3.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-29T15:21:57Zoai:sedici.unlp.edu.ar:10915/86650Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-29 15:21:58.103SEDICI (UNLP) - Universidad Nacional de La Platafalse |
| dc.title.none.fl_str_mv |
DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutations |
| title |
DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutations |
| spellingShingle |
DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutations Abba, Martín Carlos Ciencias Médicas DMBA Mammary tumors MPA Pik3ca Pten |
| title_short |
DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutations |
| title_full |
DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutations |
| title_fullStr |
DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutations |
| title_full_unstemmed |
DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutations |
| title_sort |
DMBA induced mouse mammary tumors display high incidence of activating Pik3ca<sup>H1047</sup> and loss of function Pten mutations |
| dc.creator.none.fl_str_mv |
Abba, Martín Carlos Zhong, Yi Lee, Jaeho Kil, Hyunsuk Lu, Yue Takata, Yoko Simper, Melissa S. Gaddis, Sally Shen, Jianjun Aldaz, C. Marcelo |
| author |
Abba, Martín Carlos |
| author_facet |
Abba, Martín Carlos Zhong, Yi Lee, Jaeho Kil, Hyunsuk Lu, Yue Takata, Yoko Simper, Melissa S. Gaddis, Sally Shen, Jianjun Aldaz, C. Marcelo |
| author_role |
author |
| author2 |
Zhong, Yi Lee, Jaeho Kil, Hyunsuk Lu, Yue Takata, Yoko Simper, Melissa S. Gaddis, Sally Shen, Jianjun Aldaz, C. Marcelo |
| author2_role |
author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Ciencias Médicas DMBA Mammary tumors MPA Pik3ca Pten |
| topic |
Ciencias Médicas DMBA Mammary tumors MPA Pik3ca Pten |
| dc.description.none.fl_txt_mv |
Controversy always existed on the utility of chemically induced mouse mammary carcinogenesis models as valid equivalents for the study of human breast cancer. Here, we performed whole exome and RNA sequencing on long latency mammary tumors (218 ± 27 days) induced by the carcinogen 7,12-Dimethylbenzathracene (DMBA) and short latency tumors (65 ± 11 days) induced by the progestin Medroxyprogesterone Acetate (MPA) plus DMBA in CD2F1 mice. Long latency tumors displayed a high frequency of <i>Pi3kca</i> and/or <i>Pten</i> mutations detected in 11 of 13 (85%) long latency cases (14/22, 64% overall). Eighty-two percent (9/11) of tumors carried the <i>Pik3ca</i> H1047L/R hotspot mutation, as frequently found in human breast cancer. These tumors were luminallike and mostly ER/PR+, as in humans. Transcriptome profiling indicated a significant activation of the PI3K-Akt pathway (p=3.82e-6). On the other hand MPA+DMBA induced short latency tumors displayed mutations in cancer drivers not commonly found mutated in human breast cancer (e.g. <i>Hras</i> and <i>Apc</i>). These tumors were mostly basal-like and MPA exposure led to <i>Rankl</i> overexpression (60 fold induction) and immunosuppressive gene expression signatures. In summary, long latency DMBA induced mouse mammary tumors reproduce the molecular profile of human luminal breast carcinomas representing an excellent preclinical model for the testing of PIK3CA/Akt/mTOR pathway inhibitory therapies and a good platform for the developing of additional preclinical tools such as syngeneic transplants in immunocompetent hosts. Facultad de Ciencias Médicas Centro de Investigaciones Inmunológicas Básicas y Aplicadas |
| description |
Controversy always existed on the utility of chemically induced mouse mammary carcinogenesis models as valid equivalents for the study of human breast cancer. Here, we performed whole exome and RNA sequencing on long latency mammary tumors (218 ± 27 days) induced by the carcinogen 7,12-Dimethylbenzathracene (DMBA) and short latency tumors (65 ± 11 days) induced by the progestin Medroxyprogesterone Acetate (MPA) plus DMBA in CD2F1 mice. Long latency tumors displayed a high frequency of <i>Pi3kca</i> and/or <i>Pten</i> mutations detected in 11 of 13 (85%) long latency cases (14/22, 64% overall). Eighty-two percent (9/11) of tumors carried the <i>Pik3ca</i> H1047L/R hotspot mutation, as frequently found in human breast cancer. These tumors were luminallike and mostly ER/PR+, as in humans. Transcriptome profiling indicated a significant activation of the PI3K-Akt pathway (p=3.82e-6). On the other hand MPA+DMBA induced short latency tumors displayed mutations in cancer drivers not commonly found mutated in human breast cancer (e.g. <i>Hras</i> and <i>Apc</i>). These tumors were mostly basal-like and MPA exposure led to <i>Rankl</i> overexpression (60 fold induction) and immunosuppressive gene expression signatures. In summary, long latency DMBA induced mouse mammary tumors reproduce the molecular profile of human luminal breast carcinomas representing an excellent preclinical model for the testing of PIK3CA/Akt/mTOR pathway inhibitory therapies and a good platform for the developing of additional preclinical tools such as syngeneic transplants in immunocompetent hosts. |
| publishDate |
2016 |
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2016 |
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