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1.
Br J Surg ; 108(11): 1315-1322, 2021 11 11.
Artigo em Inglês | MEDLINE | ID: mdl-34467970

RESUMO

BACKGROUND: There is a lack of information regarding the provision of parental leave for surgical careers. This survey study aims to evaluate the experience of maternity/paternity leave and views on work-life balance globally. METHODS: A 55-item online survey in 24 languages was distributed via social media as per CHERRIES guideline from February to March 2020. It explored parental leave entitlements, attitude towards leave taking, financial impact, time spent with children and compatibility of parenthood with surgical career. RESULTS: Of the 1393 (male : female, 514 : 829) respondents from 65 countries, there were 479 medical students, 349 surgical trainees and 513 consultants. Consultants had less than the recommended duration of maternity leave (43.8 versus 29.1 per cent), no paid maternity (8.3 versus 3.2 per cent) or paternity leave (19.3 versus 11.0 per cent) compared with trainees. Females were less likely to have children than males (36.8 versus 45.6 per cent, P = 0.010) and were more often told surgery is incompatible with parenthood (80.2 versus 59.5 per cent, P < 0.001). Males spent less than 20 per cent of their salary on childcare and fewer than 30 hours/week with their children. More than half (59.2 per cent) of medical students did not believe a surgical career allowed work-life balance. CONCLUSION: Surgeons across the globe had inadequate parental leave. Significant gender disparity was seen in multiple aspects.


Assuntos
Escolha da Profissão , Internato e Residência/estatística & dados numéricos , Licença Parental/estatística & dados numéricos , Estudantes de Medicina/estatística & dados numéricos , Cirurgiões/estatística & dados numéricos , Inquéritos e Questionários , Adulto , Atitude do Pessoal de Saúde , Feminino , Humanos , Masculino , Fatores Sexuais , Adulto Jovem
2.
Ann Oncol ; 30(4): 510-519, 2019 04 01.
Artigo em Inglês | MEDLINE | ID: mdl-30721924

RESUMO

Despite significant progress in our understanding of the etiology, biology and genetics of colorectal cancer, as well as important clinical advances, it remains the third most frequently diagnosed cancer worldwide and is the second leading cause of cancer death. Based on demographic projections, the global burden of colorectal cancer would be expected to rise by 72% from 1.8 million new cases in 2018 to over 3 million in 2040 with substantial increases anticipated in low- and middle-income countries. In this meeting report, we summarize the content of a joint workshop led by the National Cancer Institute and the International Agency for Research on Cancer, which was held to summarize the important achievements that have been made in our understanding of colorectal cancer etiology, genetics, early detection and treatment and to identify key research questions that remain to be addressed.


Assuntos
Neoplasias Colorretais , Congressos como Assunto , Carga Global da Doença/tendências , Cooperação Internacional , Carga Global da Doença/estatística & dados numéricos , Humanos , Oncologia/organização & administração , Oncologia/estatística & dados numéricos , Oncologia/tendências , National Cancer Institute (U.S.)/estatística & dados numéricos , Estados Unidos
3.
Oncogene ; 27(25): 3539-45, 2008 Jun 05.
Artigo em Inglês | MEDLINE | ID: mdl-18193083

RESUMO

Activation of the phosphatidylinositol 3'-kinase (PI3K)/AKT pathway results in an increase in cell proliferation and survival. Somatic mutations within the PI3K catalytic subunit, PIK3CA are common cause of increasing PI3K activity and are believed to be oncogenic in many cancer types. Few reports addressed the association between PIK3CA mutations and tumor progression specifically in microsatellite instable (MSI) colorectal cancer (CRC). In the present study, we have evaluated PIK3CA mutational status in a series of 410 Middle Eastern CRC and 13 colon cell lines to study the prevalence of PIK3CA mutations in MSI cases, PTEN expression in CRC and possibility of therapeutic targeting of this set of patients. PIK3CA mutations were found in four of the cell lines tested and 51 colorectal carcinomas (12.2%). Three of these four mutated cell lines were MSI. PTEN was inactivated in 66.1% of the CRC. Furthermore, we observed a strong association between PIK3CA mutations and MSI status (P=0.0046) while PTEN loss was more frequent in microsatellite stable (MSS) CRC (P=0.043). A high prevalence of genetic alterations in PI3K/AKT pathway in Saudi cohort of CRC, predominance of PIK3CA mutations in the MSI subgroup and their possible involvement in development/progression of this subset of CRC are some of the significant findings of our study.


Assuntos
Carcinoma/metabolismo , Neoplasias Colorretais/etnologia , Neoplasias Colorretais/genética , Mutação , Fosfatidilinositol 3-Quinases/genética , Linhagem Celular Tumoral , Classe I de Fosfatidilinositol 3-Quinases , Estudos de Coortes , Análise Mutacional de DNA , Progressão da Doença , Perfilação da Expressão Gênica , Humanos , Modelos Biológicos , Fenótipo , Fosfatidilinositol 3-Quinases/metabolismo , Arábia Saudita , Proteína Supressora de Tumor p53/genética
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