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1.
Journal of Integrative Medicine ; (12): 555-560, 2021.
Article in English | WPRIM | ID: wpr-922529

ABSTRACT

Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) is a rare adverse cutaneous reaction with a low incidence and high mortality. Despite posing a serious threat to patients' health and lives, there is no high-quality evidence for a standard treatment regimen. Here we report the case of a 62-year-old man with stage IV pancreatic cancer who experienced immunotherapy-induced SJS/TEN. After consensus-based regular treatments at a local hospital, his symptoms became worse. Thus, he consented to receive Chinese herbal medicine (CHM) therapy. The affected parts of the patient were treated with the CHM Pi-Yan-Ning which was applied externally for 20 min twice a day. After 7 days of treatment, the dead skin began peeling away from the former lesions that had covered his hands, feet, and lips, indicating that skin had regenerated. After 12 days of treatment, the patient's skin was completely recovered. In this case, SJS/TEN was successfully treated with Pi-Yan-Ning, suggesting that there might be tremendous potential for the use of Pi-Yan-Ning in the treatment of severe skin reactions to drug treatments. Further basic investigations and clinical trials to explore the mechanism and efficacy are needed.


Subject(s)
Humans , Male , Middle Aged , Drugs, Chinese Herbal/therapeutic use , Immunologic Factors , Incidence , Skin , Stevens-Johnson Syndrome/etiology
2.
Chinese journal of integrative medicine ; (12): 812-819, 2019.
Article in English | WPRIM | ID: wpr-777098

ABSTRACT

OBJECTIVE@#To evaluate the association between Chinese medicine (CM) therapy and disease-free survival (DFS) outcomes in postoperative patients with non-small cell lung cancer (NSCLC).@*METHODS@#This multiple-center prospective cohort study was conducted in 13 medical centers in China. Patients with stage I, II, or IIIA NSCLC who had undergone radical resection and received conventional postoperative treatment according to the National Comprehensive Cancer Network (NCCN) guidelines were recruited. The recruited patients were divided into a CM treatment group and a control group according to their wishes. Patients in the CM treatment group received continuous CM therapy for more than 6 months or until disease progression. Patients in the control group received CM therapy for less than 1 month. Follow-up was conducted over 3 years. The primary outcome was DFS, with recurrence/metastasis rates as a secondary outcome.@*RESULTS@#Between May 2013 and August 2016, 503 patients were enrolled into the cohort; 266 were classified in the CM treatment group and 237 in the control group. Adjusting for covariates, high exposure to CM was associated with better DFS [hazard ratio (HR) = 0.417, 95% confidential interval (CI): 0.307-0.567)]. A longer duration of CM therapy (6-12 months, 12-18 months, >24 months) was associated with lower recurrence and metastasis rates (HR = 0.225, 0.119 and 0.083, respectively). In a subgroup exploratory analysis, CM therapy was also a protective factor of cancer recurrence and metastasis in both stage I-IIIA (HR=0.50, 95% CI: 0.37-0.67) and stage IIIA NSCLC postoperative patients (HR = 0.48, 95% CI: 0.33-0.71), DFS was even longer among CM treatment group patients.@*CONCLUSIONS@#Longer duration of CM therapy could be considered a protective factor of cancer recurrence and metastasis. CM treatment is associated with improving survival outcomes of postoperative NSCLC patients in China. (Registration No. ChiCTR-OOC-14005398).

3.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 572-577, 2015.
Article in Chinese | WPRIM | ID: wpr-297382

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect of aqueous extract of Taxus chinensis var. mairei (AETC) combined Erlotnib on the growth of A549 xenograft in nude mice and its mechanism.</p><p><b>METHODS</b>The xenograft model in nude mice was established by inoculating A549 cells subcutaneously. BALB/c nude mice bearing A549 xenograft were randomly divided into six groups, i.e., the low dose Erlotinib group (A) , the standard dose Erlotnib group (B) , the low dose Erlotinib combined AETC group (C), the standard dose Erlotnib combined AETC group (D), the AETC group (E), the control group (F), 12 in each group. Different medication was performed for 7 successive weeks after 24 h. One mL blood was withdrawn and tumor tissues taken. The tumor inhibition rate was calculated. The combined effect was analyzed by Jin's Formula [Q = Ea + b/(Ea + Eb-Ea x Eb) ]. mRNA and protein expression levels of epidermal growth factor receptor (EGFR), cyclooxygenase-2 (COX-2), and B cell lymphoma-2 (Bcl-2) in xenografts were detected using real-time RT-PCR and ELISA.</p><p><b>RESULTS</b>Compared with Group F, the xenograft weight was obviously lowered in Group B-E (P < 0.05, P < 0.01). The q value was 0.92 in Group C and 0.96 in Group D, which was obtained by simple adding of the two drugs. Compared with Group F, EG- FR mRNA expression in Group D and E, COX-2 mRNA expression in Group A-E; Bcl-2 mRNA expression in Group B-D; COX-2 protein expression in Group B-E; Bcl-2 protein expression in Group C and D were obviously lowered with statistical difference (P < 0.05, P < 0.01).</p><p><b>CONCLUSIONS</b>AETC combined low dose and standard dose Erlotinib had synergistic effect on tumor inhibition. Its mechanism might be associated with down-regulating mRNA and protein expression levels of COX-2 and Bcl-2.</p>


Subject(s)
Animals , Mice , Antineoplastic Agents , Pharmacology , Antineoplastic Combined Chemotherapy Protocols , Pharmacology , Cell Line, Tumor , Cyclooxygenase 2 , Metabolism , Drugs, Chinese Herbal , Pharmacology , Enzyme Inhibitors , Pharmacology , Erlotinib Hydrochloride , Pharmacology , Heterografts , Lung Neoplasms , Mice, Inbred BALB C , Mice, Nude , ErbB Receptors , Metabolism , Taxus , Transplantation, Heterologous
4.
China Journal of Chinese Materia Medica ; (24): 3549-3553, 2013.
Article in Chinese | WPRIM | ID: wpr-291328

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect of aqueous extract of Taxus chinensis var. mairei (AETC) on the growth of A549 lung cancer xenografts in nude mice and its mechanism.</p><p><b>METHOD</b>The A549 lung cancer xenograft model was established, and then randomly divided into the control group, and low, middle and high dose AETC experiment groups. After 24 hours, they were orally administered with normal saline and drugs of the same volume for seven weeks. The length and width of the xenografts were measured every three days, and the xenograft growth curve was drawn. The nude mice were sacrificed after the administration for seven weeks, and their xenografts were collected to cultivate the anti-tumor rate. Real-time PCR and Western-blot were adopted to detect mRNA and protein levels.</p><p><b>RESULT</b>All of AETC experiment groups showed a significant anti-tumor effect (P < 0.05). Compared with the control group, each experimental group showed notable reduction in EGFR and Survivin mRNA in xenograft tissues (P < 0.05), with no significant change in VEGF mRNA level. The analysis on gray value ratio showed that EGFR mRNA were down-regulated (P < 0.05) in xenograft tissues in all experimental groups, but with no statistical significance in difference, and Survivin and p-EGFR were significantly down-regulated.</p><p><b>CONCLUSION</b>AETC has not significant effect on angiogenesis, but may have the inhibitory effect on xenograft growth by inhibiting Survivin protein and EGFR phosphorylation.</p>


Subject(s)
Animals , Humans , Male , Mice , Cell Line, Tumor , Cell Proliferation , Drugs, Chinese Herbal , Growth Inhibitors , Lung Neoplasms , Drug Therapy , Genetics , Metabolism , Taxus , Chemistry , Vascular Endothelial Growth Factor A , Genetics , Metabolism , Xenograft Model Antitumor Assays
5.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 805-809, 2013.
Article in Chinese | WPRIM | ID: wpr-287464

ABSTRACT

<p><b>OBJECTIVE</b>To study the inhibitory effects of Taxus chinensis var. mairei Aqueous Extract (TAE) on SGC-7901 and MCF-7 cells, and to explore its mechanisms.</p><p><b>METHODS</b>The inhibitory effects of TAT and Paclitaxel on the proliferation of SGC-7901 and MCF-7 cells were tested by MTT method. Their effects on the morphology of SGC-7901 and MCF-7 cells were observed by microscope. Its effects on the cell apoptosis were detected by flow cytometry.</p><p><b>RESULTS</b>The TAE had inhibitory effects on the proliferation of tumor cells, and its mechanisms were correlated to inducing the apoptosis of tumor cells.</p><p><b>CONCLUSION</b>TAE had inhibitory effects on the proliferation of tumor cells.</p>


Subject(s)
Humans , Apoptosis , Cell Line, Tumor , Cell Proliferation , MCF-7 Cells , Plant Extracts , Pharmacology , Taxus , Chemistry
6.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 1243-1247, 2011.
Article in Chinese | WPRIM | ID: wpr-299030

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the apoptosis inducing effects of aqueous extract of Taxus chinensis (AETC) in human lung cancer cell A549 and its molecular mechanisms.</p><p><b>METHODS</b>Using MTT assay, the inhibition of AETC on the proliferation of A549 cells was detected. The apoptosis was detected by light and electron microscopy, and Annexin V-FITC/PI staining. The expressions of ERK1/2, JNK1/2, and survivin were analyzed by Western blot.</p><p><b>RESULTS</b>AETC could inhibit the proliferation of A549 cells. Obvious apoptotic cells could be seen under light and electron microscope in AETC treated A549 cells. AETC's induction on the cell apoptosis was further confirmed by Annexin V-FITC/PI labeled quantitative detection. Western blot assay showed that AETC could decrease the survivin expressions. AETC showed no effects on ERK1/2 or JNK1/2 protein expressions.</p><p><b>CONCLUSION</b>AETC could significantly inhibit the proliferation of A549 cells and induce the apoptosis, which was mainly achieved through regulating the expressions of survivin.</p>


Subject(s)
Humans , Apoptosis , Cell Line, Tumor , Cell Proliferation , Extracellular Signal-Regulated MAP Kinases , Metabolism , Inhibitor of Apoptosis Proteins , Metabolism , Lung Neoplasms , Pathology , MAP Kinase Signaling System , Plant Extracts , Pharmacology , Taxus
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