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1.
Mol Cancer ; 22(1): 114, 2023 07 17.
Artigo em Inglês | MEDLINE | ID: mdl-37460925

RESUMO

BACKGROUND: Malignant Pleural Mesothelioma (MPM) is a dreadful disease escaping the classical genetic model of cancer evolution and characterized by wide heterogeneity and transcriptional plasticity. Clinical evolution of MPM is marked by a progressive transdifferentiation that converts well differentiated epithelioid (E) cells into undifferentiated and pleomorphic sarcomatoid (S) phenotypes. Catching the way this transition takes place is necessary to understand how MPM develops and progresses and it is mandatory to improve patients' management and life expectancy. Bulk transcriptomic approaches, while providing a significant overview, failed to resolve the timing of this evolution and to identify the hierarchy of molecular events through which this transition takes place. METHODS: We applied a spatially resolved, high-dimensional transcriptomic approach to study MPM morphological evolution. 139 regions across 8 biphasic MPMs (B-MPMs) were profiled using the GeoMx™Digital Spatial Profiler to reconstruct the positional context of transcriptional activities and the spatial topology of MPM cells interactions. Validation was conducted on an independent large cohort of 84 MPMs by targeted digital barcoding analysis. RESULTS: Our results demonstrated the existence of a complex circular ecosystem in which, within a strong asbestos-driven inflammatory environment, MPM and immune cells affect each other to support S-transdifferentiation. We also showed that TGFB1 polarized M2-Tumor Associated Macrophages foster immune evasion and that TGFB1 expression correlates with reduced survival probability. CONCLUSIONS: Besides providing crucial insights into the multidimensional interactions governing MPM clinical evolution, these results open new perspectives to improve the use of immunotherapy in this disease.


Assuntos
Neoplasias Pulmonares , Mesotelioma Maligno , Mesotelioma , Neoplasias Pleurais , Humanos , Mesotelioma/genética , Mesotelioma/terapia , Transcriptoma , Ecossistema , Neoplasias Pleurais/genética , Neoplasias Pleurais/terapia , Neoplasias Pulmonares/genética , Prognóstico , Biomarcadores Tumorais/genética , Imunoterapia
2.
J Endocrinol Invest ; 45(4): 753-762, 2022 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-34792796

RESUMO

PURPOSE: Hypogonadism was described in high number of male subjects with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. In this study, we investigated whether low testosterone (T) values may influence the clinical presentation and outcome of SARS-CoV-2-related pneumonia in a large population of adult males with coronavirus disease 19 (COVID-19). METHODS: Two hundred twenty one adult males hospitalized for COVID-19 at the IRCCS Humanitas Research Hospital, Rozzano-Milan (Italy) were consecutively evaluated for arterial partial pressure oxygen (PaO2)/fraction of inspired oxygen (FiO2) ratio, serum T and inflammatory parameters at study entry, need of ventilation during hospital stay and in-hospital mortality. RESULTS: Subjects low T values (< 8 nmol/L; 176 cases) were significantly older (P = 0.001) and had higher serum interleukin-6 (P = 0.001), C-reactive protein (P < 0.001), lactate dehydrogenase (P < 0.001), ferritin (P = 0.012), lower P/F ratio (P = 0.001), increased prevalence of low T3 syndrome (P = 0.041), acute respiratory insufficiency (P < 0.001), more frequently need of ventilation (P < 0.001) and higher mortality rate (P = 0.009) compared to subjects with higher T values. In the multivariable regression analyses, T values maintained significant associations with acute respiratory insufficiency (odds ratio [OR] 0.85, 95% confidence interval [CI] 0.79-0.94; P < 0.001 and in-hospital mortality (OR 0.80, 95% CI 0.69-0.95; P = 0.009), independently of age, comorbidities, thyroid function and inflammation. CONCLUSION: Low T levels values are associated with unfavorable outcome of COVID-19. Prospective studies are needed to evaluate the long-term outcomes of hypogonadism related to COVID-19 and the clinical impact of T replacement during and after acute illness.


Assuntos
COVID-19/complicações , Insuficiência Respiratória/etiologia , Testosterona/sangue , Adulto , Idoso , Idoso de 80 Anos ou mais , Biomarcadores/sangue , COVID-19/sangue , COVID-19/mortalidade , Hospitalização , Humanos , Itália/epidemiologia , Masculino , Pessoa de Meia-Idade , Insuficiência Respiratória/sangue , Insuficiência Respiratória/mortalidade , Taxa de Sobrevida
3.
Chirurgie ; 116(1): 89-97; discussion 97-8, 1990.
Artigo em Francês | MEDLINE | ID: mdl-2226044

RESUMO

70 cases of carcinoma of the anus are described in a retrospective study. All patients had been operated, since surgical treatment was regarded as the method of choice at that time. Our work therefore consists in assessing the role of surgery in the treatment of such carcinomas. In the initial forms, extended sphincter saving exeresis allowed excellent results (100% survival over a 1- to 10-year follow-up). In more advanced lesions, treated with abdominoperineal resection, the survival rate was 50% after 5 years. The same figure was obtained in case of extension to the female genital organs (the invasion of which is not a pejorative sign), while the prognosis was considerably worsened for the patients who had had lymph node resection due to invasion of inguinal nodes (20% survived after 5 years). Local surgical exeresis currently is as valuable as radiation therapy, but the latter is clearly indicated for advanced carcinomas, for which mutilating surgery has not demonstrated its superiority.


Assuntos
Adenocarcinoma/cirurgia , Neoplasias do Ânus/cirurgia , Carcinoma de Células Escamosas/cirurgia , Carcinoma de Células de Transição/cirurgia , Adenocarcinoma/terapia , Neoplasias do Ânus/terapia , Carcinoma de Células Escamosas/terapia , Carcinoma de Células de Transição/terapia , Seguimentos , Humanos , Melanoma/cirurgia , Melanoma/terapia , Estudos Retrospectivos
4.
Ophthalmic Paediatr Genet ; 5(1-2): 39-49, 1985 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-4058871

RESUMO

A renal syndrome with tapetoretinal degeneration and closed-angled glaucoma and transmitted in an autosomal dominant pattern is described. The precise classification of this syndrome is unclear but may represent a variant of Alport syndrome or nephronophthisis (Senior-Biochis syndrome).


Assuntos
Glaucoma/genética , Nefropatias/genética , Retinose Pigmentar/genética , Adulto , Idoso , Criança , Feminino , Genes Dominantes , Glaucoma/complicações , Humanos , Nefropatias/complicações , Masculino , Pessoa de Meia-Idade , Retinose Pigmentar/complicações , Síndrome , Campos Visuais
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