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1.
China Pharmacy ; (12): 2550-2555, 2023.
Article in Chinese | WPRIM | ID: wpr-997018

ABSTRACT

Autoimmune diseases(ADs) are diseases in which the body’s immune tolerance is impaired, causing damage to its tissues. The pro-inflammatory helper T cell 17 (Th17) and anti-inflammatory regulatory T cell (Treg) are functionally antagonistic to each other, and the immune imbalance between them and the imbalance of related inflammatory factors are closely related to the occurrence of a variety of ADs. Plenty of evidence has shown that gut microbiota can regulate Th17/Treg differentiation, rebuild immune tolerance and delay the ADs process through regulating cytokine production, transcription factor expression and energy metabolism. This paper reviews the intervention effects of traditional Chinese medicine(TCM) monomers on the common ADs by regulating Th17/Treg differentiation balance based on intestinal flora: ulcerative colitis,rheumatoid arthritis and diabetes mellitus type 1. It is found that its mechanism of action may be to restore the balance of pro-inflammatory factors and anti-inflammatory factors to alleviate intestinal mucosal barrier damage, reduce synovial angiogenesis and improve pancreatic β cell destruction, which provides some ideas for the prevention and treatment of ADs with integrated traditional Chinese and western medicine.

2.
Chinese Journal of Pathology ; (12): 298-302, 2017.
Article in Chinese | WPRIM | ID: wpr-808695

ABSTRACT

Objective@#To investigate the clinicopathologic features and genetic profile of large cell lung carcinoma (LCC) redefined by new classification.@*Methods@#Basing on 2015 WHO classification criteria in redefining large cell lung carcinoma, the expression of specific markers (TTF1, Napsin A, p40, CK5/6, CK, vimentin and ZEB1) was detected by immunohistochemistry and D-PAS staining in 303 surgically-removed lung specimens previously diagnosed as large cell lung carcinoma. The clinicopathologic and genetic characteristics (including EGFR, KRAS, BRAF, ALK and ROS1 gene mutation) were analyzed.@*Results@#Based on the new definition of LCC, 116 cases (116/303, 38.3%) of LCC formerly diagnosed were reclassified as solid adenocarcinoma, 49 cases (49/303, 16.2%) as squamous cell carcinoma, 6 cases (6/303, 2.0%) as adenosquamous carcinoma, 22 cases (22/303, 7.3%) as spindle cell carcinoma and only 110 cases (110/303, 36.3%) as large cell carcinoma. Redefined LCCs were characterized as middle-age (range 40-80), male (102/110, 92.7%) and smoking patients (64/110, 58.2%) with intermediate-advanced stage. Among 110 cases, 9 cases with EGFR mutation and 10 cases with KRAS mutation and 1 case with ALK fusion were found. No BRAF and ROS1 alterations were identified.@*Conclusions@#According to the new classification, LCCs formerly diagnosed are mostly reclassified as adenocarcinoma and non-keratinizing squamous cell carcinoma. The newly defined LCC may significantly benefit from clinical therapy.

3.
Chinese Journal of Pathology ; (12): 644-647, 2015.
Article in Chinese | WPRIM | ID: wpr-358946

ABSTRACT

<p><b>OBJECTIVE</b>To study the expression of squamous cell markers p63, p40 and CK5/6 in small cell carcinoma of lung (SCLC).</p><p><b>METHODS</b>Immunohistochemical study for squamous cell markers (p63, p40 and CK5/6), neuroendocrine markers (chromogranin A, synaptophysin and CD56) and TTF1 was carried out in 283 cases of SCLC. The diagnostic value of these markers was evaluated.</p><p><b>RESULTS</b>The expression rate of p63, p40 and CK5/6 were 20.7% (54/261), 7.9% (5/63) and 0.5% (1/221), respectively in the cases of SCLC studied. Amongst the squamous cell markers, CK5/6 had the lowest rate of positivity (P < 0.01). On the other hand, chromogranin A, synaptophysin and CD56 were positive in 61.8% (170/275), 85.5% (242/283) and 89.2% (248/278), respectively. The positivity rate for chromogranin A was lower than that for synaptophysin and CD56 (P < 0.01). TTF1 was expressed in 77.2% (217/281).</p><p><b>CONCLUSIONS</b>p63 and p40 are expressed in a subset of SCLC. In contrast, CK5/6 is rarely positive in SCLC. An immunohistochemical panel of CK5/6, synaptophysin and CD56 is recommended for differential diagnosis of SCLC.</p>


Subject(s)
Humans , CD56 Antigen , Genetics , Metabolism , Chromogranin A , Genetics , Metabolism , DNA-Binding Proteins , Genetics , Metabolism , Diagnosis, Differential , Keratin-5 , Genetics , Metabolism , Keratin-6 , Genetics , Metabolism , Lung Neoplasms , Genetics , Metabolism , Small Cell Lung Carcinoma , Genetics , Metabolism , Synaptophysin , Genetics , Metabolism , Transcription Factors , Genetics , Metabolism , Tumor Suppressor Proteins , Genetics , Metabolism
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