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1.
Arkh Patol ; 86(5): 5-14, 2024.
Artigo em Russo | MEDLINE | ID: mdl-39434522

RESUMO

Lung cancer occupies a leading position in the structure of global cancer morbidity and mortality, due to the biological properties of the key pool of tumor cells - cancer stem cells (CSCs). The effects of SARS-CoV2 on tumor CSCs and its niche have not been studied. OBJECTIVE: To study CSCs in lung adenocarcinomas after COVID19. MATERIAL AND METHODS: Surgical material from lung adenocarcinoma from 12 patients who had a new coronavirus infection and from 12 patients who did not have COVID19 was examined. Analysis of clinical and anamnestic data, macroscopic and microscopic examination of tumor samples and adjacent intact tissue, immunohistochemical reactions using antibodies to virus proteins and CSC markers ALDH1, CD133 and CD34 were performed. RESULTS: Adenocarcinoma samples from patients in the main group showed a significant increase in the number of cells expressing the CSCs markers ALDH1, CD133 and CD34 compared to adenocarcinoma samples from control group patients without SARS-CoV2 infection. We found an increase in the number of CSCs in patients with adenocarcinoma metastasis in lymph nodes in both the main and control groups. CSCs of lung adenocarcinomas from SARS-CoV2 survivors contain virus proteins Nucleocapside and Spike protein. CONCLUSIONS: We found an increase in the number of CSCs with expression of ALDH1, CD133 and CD34 in lung adenocarcinoma in patients with new coronavirus infection. Increased number of ALDH1+, CD133+ CD34+ CSCs in tumor tissue enhance the metastatic potential of lung adenocarcinoma. The Nucleocapsid and Spike proteins of SARS-CoV2 virus are detectable in lung tissue from patients with new coronavirus infection, both in adenocarcinoma cells, CSCs, and in type II pneumocytes, macrophages, and endothelial cells, suggesting prolonged persistence of the virus proteins and probably the virus.


Assuntos
Antígeno AC133 , Adenocarcinoma de Pulmão , Família Aldeído Desidrogenase 1 , Antígenos CD34 , COVID-19 , Neoplasias Pulmonares , Células-Tronco Neoplásicas , Retinal Desidrogenase , SARS-CoV-2 , Humanos , Células-Tronco Neoplásicas/patologia , Células-Tronco Neoplásicas/virologia , Células-Tronco Neoplásicas/metabolismo , Antígeno AC133/metabolismo , COVID-19/patologia , COVID-19/virologia , COVID-19/metabolismo , Masculino , Neoplasias Pulmonares/virologia , Neoplasias Pulmonares/patologia , Neoplasias Pulmonares/metabolismo , Pessoa de Meia-Idade , Feminino , Adenocarcinoma de Pulmão/patologia , Adenocarcinoma de Pulmão/virologia , Adenocarcinoma de Pulmão/metabolismo , Adenocarcinoma de Pulmão/imunologia , Família Aldeído Desidrogenase 1/metabolismo , Idoso , Antígenos CD34/metabolismo , Retinal Desidrogenase/metabolismo , Pulmão/virologia , Pulmão/patologia , Pulmão/metabolismo , Biomarcadores Tumorais/metabolismo , Proteínas Virais/metabolismo
2.
Arkh Patol ; 86(3): 46-51, 2024.
Artigo em Russo | MEDLINE | ID: mdl-38881005

RESUMO

Alveolar proteinosis is a rare lung disease characterized by the accumulation of protein-lipid complexes in the alveoli due to impaired surfactant utilization by alveolar macrophages. The frequency is from 2 to 4 cases per 1 million adult population. We present an observation of pulmonary alveolar proteinosis in a patient with a history of coronavirus pneumonia.


Assuntos
COVID-19 , Proteinose Alveolar Pulmonar , SARS-CoV-2 , Humanos , Proteinose Alveolar Pulmonar/patologia , COVID-19/complicações , Masculino , Pessoa de Meia-Idade , Feminino , Macrófagos Alveolares/virologia , Macrófagos Alveolares/patologia , Macrófagos Alveolares/metabolismo
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