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1.
Arch Virol ; 162(9): 2855-2860, 2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28597068

RESUMO

In Brazil, most studies of intra-type variants of human papillomavirus (HPV) have focused on HPV16 and HPV18, but other high-risk HPV types have not been studied. Here, we report the prevalence of lineages and variants of HPV35, HPV45 and HPV58 in cervical cancers from the Amazonian and Southeast Brazilian regions. The most frequent sublineages were A1 for HPV35, B2 for HPV45, and A2 for HPV58. The Southeast region had a higher frequency of the B2 sublineage of HPV45, and for HPV35, the genetic and nucleotide sequence diversity were higher in the Southeast region, suggesting that regional factors are influencing the diversity and lineage prevalence.


Assuntos
Variação Genética , Papillomaviridae/classificação , Papillomaviridae/genética , Infecções por Papillomavirus/complicações , Infecções por Papillomavirus/virologia , Neoplasias do Colo do Útero/epidemiologia , Neoplasias do Colo do Útero/virologia , DNA Viral/genética , Feminino , Humanos , Infecções por Papillomavirus/epidemiologia , Filogenia
2.
J Med Virol ; 88(7): 1279-87, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26694554

RESUMO

Cervical cancer is the fourth most common cancer among women, and ∼70-80% of these cancers are associated with two human papillomavirus types: HPV16 and HPV18. Several studies have reported that intra-type diversity is associated with the progression of infection to invasive cancer. Herein, we report the genetic diversity of HPV16 and HPV18 in a cohort of 594 Brazilian women with invasive cervical cancer and describe the prevalence of lineages and intra-type diversity prior to the implementation of the public immunization program in Brazil. HPV detection and genotyping were performed using PCR, PGMY/GP primers, and DNA extracted from fresh tumors. The HPV16 (378 women) and HPV18 (80 women) lineages were identified by PCR and sequencing of the LCR and E6 fragments, followed by SNV comparison and phylogenetic analysis. In our cohort, was found a higher frequency of the lineage A (in 217 women), followed by lineage D (in 97 women) and lineages B and C (in 10 women each) for HPV16; and a higher frequency of lineage A (in 56 women) followed by lineage B (in 15 women) in HPV18. The genetic diversity of HPV16 indicated a recent expansion of specific variants or a selective advantage that is associated with invasive cancer; this pattern was not observed for HPV18.


Assuntos
Variação Genética , Papillomavirus Humano 16/genética , Papillomavirus Humano 18/genética , Neoplasias do Colo do Útero/virologia , Adulto , Idoso , Brasil/epidemiologia , DNA Viral/genética , Proteínas de Ligação a DNA/genética , Feminino , Genoma Viral , Genótipo , Papillomavirus Humano 16/isolamento & purificação , Papillomavirus Humano 18/classificação , Papillomavirus Humano 18/isolamento & purificação , Humanos , Pessoa de Meia-Idade , Invasividade Neoplásica , Proteínas Oncogênicas Virais/genética , Filogenia , Prevalência , Proteínas Repressoras/genética , Fatores de Risco , Neoplasias do Colo do Útero/epidemiologia , Neoplasias do Colo do Útero/patologia , Adulto Jovem
3.
BMC Urol ; 15: 13, 2015 Feb 24.
Artigo em Inglês | MEDLINE | ID: mdl-25887354

RESUMO

BACKGROUND: The human papillomavirus (HPV) prevalence in males has been reported to be between 3.6% and 84%, depending specially on the socioeconomic status. HPV infection has been related as a risk factor for penile cancer. This is a rare tumor, and other risk factors include lack of personal hygiene and men who have not undergone circumcision. Penile cancer is less than 1% of cancers in men in the United States, however, is much more common in some parts of Asia, Africa, and South America, where it accounts for up to 10% of cancers in men. This study aimed to determine the prevalence of HPV-DNA in penile cancers in São Luís, Brazil and to correlate the virus presence to histopathological factors. METHODS: Tumor paraffin samples of 76 patients with penile carcinoma were tested in order to establish the prevalence and distribution of genotypic HPV using PCR/Nested and automated sequencing. To evaluate the association between HPV types and other clinical and morphological variables, a nonparametric ANOVA was performed using a Kruskal Wallis test, and statistical significance was determined to a value of p < 0.05. RESULTS: The average age of patients at the time of diagnosis was 66 years ± 17.10. Regarding location, 65.79% of the tumors were located in the glans, and the most common types were vegetative (34.21%) and squamous (98.68%). Most of the lesions ranged in size from 2.1 to 5.0 cm, presenting Jackson I stage and Broders II degree. It was observed that 32 patients had at least one invaded and/or infiltrated structure. Lymph node involvement was observed in 19.76% of the patients, and 21.05% showed an inflammatory process. In the molecular evaluation, HPV infection was observed in 63.15% of the lesions, and the most common type was HPV 16. CONCLUSIONS: From the statistical analysis, it can be verified that the variables were not associated with infection by the HPV virus. Although penile cancer can result from various risk factors that act in synergy, an HPV virus infection is important for the development of such neoplasm.


Assuntos
Papillomaviridae/genética , Infecções por Papillomavirus/epidemiologia , Neoplasias Penianas/epidemiologia , Neoplasias Penianas/virologia , Adulto , Distribuição por Idade , Idoso , Idoso de 80 Anos ou mais , Análise de Variância , Brasil/epidemiologia , Estudos de Coortes , Comorbidade , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Papillomaviridae/isolamento & purificação , Infecções por Papillomavirus/diagnóstico , Neoplasias Penianas/patologia , Reação em Cadeia da Polimerase , Prevalência , Estudos Retrospectivos , Medição de Risco
4.
Rev Bras Ginecol Obstet ; 45(8): e474-e479, 2023 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-37683659

RESUMO

OBJECTIVE: Similar to Human Papillomavirus (HPV) genotypes, different lineages of a genotype also have different carcinogenic capabilities. Studies have shown that specific genotype lineages of oncogenic HPV are associated with variable risks for the development of cervical intraepithelial neoplasia (CIN2/CIN3) and cervical cancer. The present study aimed to analyze the genetic diversity of the HPV16 genotype in women with CIN2/CIN3 and cervical cancer, from the northeast region of Brazil. METHODS: A cross-sectional multicenter study was conducted in the northeast region of Brazil, from 2014 to 2016. This study included 196 cases of HPV16 variants (59 and 137 cases of CIN2/CIN3 and cervical cancer, respectively). The difference of proportion test was used to compare patients with CIN2/CIN3 and cervical cancer, based on the prevalent HPV16 lineage (p < 0.05). RESULTS: According to the histopathological diagnosis, the percentage of lineage frequencies revealed a marginal difference in the prevalence of lineage A in CIN2/CIN3, compared with that in cervical cancer (p = 0.053). For lineage D, the proportion was higher in cancer cases (32.8%), than in CIN2/CIN3 cases (16.9%), with p = 0.023. CONCLUSION: HPV16 lineage A was the most frequent lineage in both CIN2/CIN3 and cervical cancer samples, while lineage D was predominant in cervical cancer, suggesting a possible association between HPV16 lineage D and cervical cancer.


OBJETIVO: Tanto os tipos quanto as linhagens do Papilomavírus Humano (HPV) parecem ter diferentes capacidades carcinogênicas e estão associados a riscos variados para o desenvolvimento de neoplasia intraepitelial cervical (NIC) e câncer de colo do útero. O presente estudo tem como objetivo analisar a diversidade genética do genótipo HPV 16 nos casos de NIC2/NIC3 e câncer de colo de útero em mulheres da região Nordeste do Brasil. MéTODOS: Estudo transversal de base hospitalar realizado na região Nordeste do Brasil no período de 2014 a 2016. A amostra foi composta por 196 casos da variante HPV-16 (59 casos de NIC2/NIC3 e 137 de câncer do colo do útero). O teste de diferença de proporção foi usado para comparar os grupos NIC2/NIC3 e câncer de colo do útero por linhagem viral em relação à prevalência da linhagem HPV-16. Foi considerada significância estatística o valor de p < 0,05. RESULTADOS: As frequências de linhagem por diagnóstico histopatológico mostraram diferença limítrofe da linhagem A no grupo NIC2/NIC3 em relação ao grupo câncer de colo de útero (p = 0,053). Por outro lado, em relação à linhagem D, houve uma proporção maior nos casos de câncer (32,8%) quando comparado ao grupo NIC2/NIC3 (16,9%) e esta diferença se mostrou estatisticamente significante (p = 0,023). CONCLUSãO: A linhagem A do HPV-16 foi a mais frequente tanto nas amostras CIN2/CIN3 quanto nas amostras de câncer de colo de útero, enquanto a linhagem D predominou no câncer de colo do útero, sugerindo uma possível associação da linhagem D de HPV-16 com câncer de colo de útero.


Assuntos
Infecções por Papillomavirus , Neoplasias do Colo do Útero , Humanos , Feminino , Neoplasias do Colo do Útero/epidemiologia , Brasil/epidemiologia , Papillomavirus Humano , Estudos Transversais , Papillomavirus Humano 16/genética , Infecções por Papillomavirus/complicações , Infecções por Papillomavirus/epidemiologia , Papillomaviridae
5.
Rev. bras. ginecol. obstet ; 45(8): 474-479, 2023. tab
Artigo em Inglês | LILACS | ID: biblio-1515062

RESUMO

Abstract Objective Similar to Human Papillomavirus (HPV) genotypes, different lineages of a genotype also have different carcinogenic capabilities. Studies have shown that specific genotype lineages of oncogenic HPV are associated with variable risks for the development of cervical intraepithelial neoplasia (CIN2/CIN3) and cervical cancer. The present study aimed to analyze the genetic diversity of the HPV16 genotype in women with CIN2/CIN3 and cervical cancer, from the northeast region of Brazil. Methods A cross-sectional multicenter study was conducted in the northeast region of Brazil, from 2014 to 2016. This study included 196 cases of HPV16 variants (59 and 137 cases of CIN2/CIN3 and cervical cancer, respectively). The difference of proportion test was used to compare patients with CIN2/CIN3 and cervical cancer, based on the prevalent HPV16 lineage (p < 0.05). Results According to the histopathological diagnosis, the percentage of lineage frequencies revealed a marginal difference in the prevalence of lineage A in CIN2/CIN3, compared with that in cervical cancer (p = 0.053). For lineage D, the proportion was higher in cancer cases (32.8%), than in CIN2/CIN3 cases (16.9%), with p = 0.023. Conclusion HPV16 lineage A was the most frequent lineage in both CIN2/CIN3 and cervical cancer samples, while lineage D was predominant in cervical cancer, suggesting a possible association between HPV16 lineage D and cervical cancer.


Resumo Objetivo Tanto os tipos quanto as linhagens do Papilomavírus Humano (HPV) parecem ter diferentes capacidades carcinogênicas e estão associados a riscos variados para o desenvolvimento de neoplasia intraepitelial cervical (NIC) e câncer de colo do útero. O presente estudo tem como objetivo analisar a diversidade genética do genótipo HPV 16 nos casos de NIC2/NIC3 e câncer de colo de útero em mulheres da região Nordeste do Brasil. Métodos Estudo transversal de base hospitalar realizado na região Nordeste do Brasil no período de 2014 a 2016. A amostra foi composta por 196 casos da variante HPV-16 (59 casos de NIC2/NIC3 e 137 de câncer do colo do útero). O teste de diferença de proporção foi usado para comparar os grupos NIC2/NIC3 e câncer de colo do útero por linhagem viral em relação à prevalência da linhagem HPV-16. Foi considerada significância estatística o valor de p < 0,05. Resultados As frequências de linhagem por diagnóstico histopatológico mostraram diferença limítrofe da linhagem A no grupo NIC2/NIC3 em relação ao grupo câncer de colo de útero (p = 0,053). Por outro lado, em relação à linhagem D, houve uma proporção maior nos casos de câncer (32,8%) quando comparado ao grupo NIC2/NIC3 (16,9%) e esta diferença se mostrou estatisticamente significante (p = 0,023). Conclusão A linhagem A do HPV-16 foi a mais frequente tanto nas amostras CIN2/CIN3 quanto nas amostras de câncer de colo de útero, enquanto a linhagem D predominou no câncer de colo do útero, sugerindo uma possível associação da linhagem D de HPV-16 com câncer de colo de útero.


Assuntos
Humanos , Feminino , Papillomavirus Humano 16
6.
Virus Res ; 232: 48-53, 2017 03 15.
Artigo em Inglês | MEDLINE | ID: mdl-28143725

RESUMO

CpG methylation at early promoter of HPV16 DNA, in the 3' end of the Long Control Region (3'LCR), has been associated to the presence of episomal forms of viral genome and, consequently, intact E1 and E2 ORFs. The DNA methylation would block the access of E2 viral protein to the E2 binding sites at early-promoter. However, is still unclear if methylation at 3'LCR of HPV16 DNA can also vary depending of other tumor characteristics in addition to viral DNA physical state. In this study, we evaluate whether the methylation level at the five CpG located at 3'LCR of HPV16 is associated to patient age and E1 and/or E2 ORFs integrity. DNA pyrosequencing was used to measure the methylation level in 69 invasive cervical cancer samples obtained from biopsies of patients attended at Brazilian National Institute of Cancer (INCA). PCR amplifications were performed to assess disruption status of E1 and E2 genes of HPV16. The methylation average per sample ranged widely, from <1 to 88.00%. Presence of intact E1/E2 genes and patient age were positively associated with average methylation in both bivariate analyses (p=0.003 and p=0.006, respectively), and multivariate analysis (p=0.002 and p=0.021, respectively), adjusted for tumor type (squamous cell carcinomas or adenocarcinomas) and HPV16 lineage. These findings showed that presence of intact E1/E2 open reading frames was associated with high levels of DNA methylation, and older patients showed higher levels of methylation than younger ones independently of viral genome disruption.


Assuntos
DNA Viral/genética , Proteínas de Ligação a DNA/genética , Papillomavirus Humano 16/genética , Proteínas Oncogênicas Virais/genética , Infecções por Papillomavirus/virologia , Neoplasias do Colo do Útero/virologia , Adenocarcinoma/patologia , Adenocarcinoma/virologia , Adulto , Fatores Etários , Sítios de Ligação , Carcinoma de Células Escamosas/patologia , Carcinoma de Células Escamosas/virologia , Ilhas de CpG , Metilação de DNA , DNA Viral/metabolismo , Proteínas de Ligação a DNA/metabolismo , Feminino , Deleção de Genes , Interações Hospedeiro-Patógeno , Papillomavirus Humano 16/metabolismo , Humanos , Pessoa de Meia-Idade , Proteínas Oncogênicas Virais/metabolismo , Fases de Leitura Aberta , Infecções por Papillomavirus/patologia , Regiões Promotoras Genéticas , Ligação Proteica , Neoplasias do Colo do Útero/patologia
7.
J Environ Public Health ; 2017: 1645074, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28512474

RESUMO

To evaluate the impact of HPV immunization and possible changes in virus type-specific prevalence associated with cervical cancer, it is important to obtain baseline information based on socioeconomic, educational, and environmental characteristics in human populations. We describe these characteristics and the type-specific HPV distribution in 1,183 women diagnosed with cervical cancer in two Brazilian healthcare institutions located at the Southeastern (Rio de Janeiro/RJ) and the Amazonian (Belém/PA) regions. Large differences were observed between women in these regions regarding economic, educational, and reproductive characteristics. The eight most frequent HPV types found in tumor samples were the following: 16, 18, 31, 33, 35, 45, 52, and 58. Some HPV types classified as unknown or low risk were found in tumor samples with single infections, HPV 83 in RJ and HPV 11, 61, and 69 in PA. The proportion of squamous cervical cancer was lower in RJ than in PA (76.3% versus 87.3%, p < 0.001). Adenocarcinoma was more frequent in RJ than in PA (13.5% versus 6.9%, p < 0.001). The frequency of HPV 16 in PA was higher in younger women (p < 0.05). The success of a cervical cancer control program should consider HPV types, local health system organization, and sociodemographic diversity of Brazilian regions.


Assuntos
Papillomaviridae/genética , Infecções por Papillomavirus/virologia , Neoplasias do Colo do Útero/virologia , Adolescente , Adulto , Idoso , Brasil/epidemiologia , Feminino , Genótipo , Humanos , Programas de Imunização/estatística & dados numéricos , Pessoa de Meia-Idade , Infecções por Papillomavirus/epidemiologia , Prevalência , Valores de Referência , Fatores Socioeconômicos , Neoplasias do Colo do Útero/epidemiologia , Adulto Jovem
8.
Rio de Janeiro; s.n; 2016. ilus.
Tese em Espanhol | LILACS, Inca | ID: biblio-943278

RESUMO

O câncer do colo do útero é o quarto tipo de câncer mais comum entre as mulheres no mundo. Sua incidência é cerca de duas vezes maior em países menos desenvolvidos em relação aos mais desenvolvidos. Dentre outros cofatores, a infecção pelo papilomavírus humano (HPV) tem sido bem documentada como fator necessário ao desenvolvimento deste tipo de câncer, sendo os tipos HPV16 e HPV18 responsáveis por aproximadamente 70-80% dos casos. A caracterização dos tipos virais mais frequentemente associados ao câncer cervical, permitiu o desenvolvimento de vacinas comerciais, atualmente disponibilizadas ou em fase de testes. Além disso, o interesse em variantes intratipo dos HPVs mais prevalentes está crescendo rapidamente, visto que evidências sugerem que essas variantes podem diferir biologicamente e etiologicamente no desenvolvimento e comportamento do tumor. Tendo em vista a relevância do câncer de colo de útero, a sua associação com diferentes tipos de HPVs, o desenvolvimento de vacinas, e o limitado número de estudos sobre a prevalência de diferentes tipos e subtipos desse câncer no Brasil, o presente projeto teve por objetivos: (1) Identificar a prevalência dos tipos de HPV identificados a partir de amostras de câncer cervical invasivo de 594 mulheres matriculadas no hospital do câncer II do Instituto Nacional do Câncer. (2) Levantar as características socioeconômicas desta coorte de pacientes. (3) Identificar a prevalência das variantes intratipo do HPV 16 e HPV 18. A detecção e genotipagem do HPV foram realizadas a partir da PCR e sequenciamento direto utilizando os iniciadores PGMY/GP, sendo identificados 370 amostras HPV 16; 77 amostras HPV 18; 33 amostras HPV45; 12 amostras HPV 35; 11 amostras HPV 58; 8 amostras HPV 73 e HPV52, respectivamente; 7 amostras HPV31 e HPV33, respectivamente; 6 amostras HPV 59 e HPV 39, respectivamente; duas amostras HPV 26, HPV 51, HPV 56 e HPV 68, respectivamente e, por fim, 1 amostra...


Cervical cancer is the forth most common cancer among women worldwide. The incidence isapproximately two times higher in less developed countries than in the more developed. Among other cofactors, infection with human papillomavirus (HPV) has been well documented as a necessary factor for the development of this cancer, and the HPV16 and HPV18 types account for approximately 70-80% of cases. The characterization of the virus types most commonly associated with cervical cancer has enabled the development of commercial vaccines currently available or being tested. Moreover, the interest invariants of the most prevalent HPV is rapidly growing, since evidence suggests that these variants maydiffer biologically and epidemiologically in the development and tumor behavior. Considering the importance of cervical cancer, its association with different types of HPV, vaccine development, and the limited number of studies on the prevalence of different types and subtypes of cervical cancer in Brazil, this study aimed to: (1) identify the prevalence of HPV types identified from invasive cervical cancer samplesfrom 594 women enrolled in the cancer hospital II of the National Cancer Institute...


Assuntos
Feminino , Institutos de Câncer , Genótipo , Papillomaviridae , Neoplasias Uterinas
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