scholarly journals The HLJ1 -targeting drug screening identified Chinese herb andrographolide that can suppress tumour growth and invasion in non-small-cell lung cancer

2013 ◽  
Vol 34 (5) ◽  
pp. 1069-1080 ◽  
Author(s):  
Yi-Hua Lai ◽  
Sung-Liang Yu ◽  
Hsuan-Yu Chen ◽  
Chi-Chung Wang ◽  
Huei-Wen Chen ◽  
...  
2020 ◽  
Vol 11 (8) ◽  
pp. 2279-2290
Author(s):  
Jing‐Hua Chen ◽  
Xiang‐Peng Chu ◽  
Jia‐Tao Zhang ◽  
Qiang Nie ◽  
Wen‐Fang Tang ◽  
...  

2012 ◽  
Vol 30 (15_suppl) ◽  
pp. e13526-e13526
Author(s):  
Siyu Chen ◽  
Wei Tian ◽  
Ai-Hong Ma ◽  
Sonal Desai ◽  
Krysteena Tolentino ◽  
...  

e13526 Background: Oridonin, a diterpenoid purified from the Chinese herb Rabdosia rubescens, has anti-inflammatory and potentially anti-tumor property. We aimed to study the antitumor effect of oridonin on a panel of human non-small cell lung cancer (NSCLC) cell lines. Methods: Human NSCLC cell lines with a wild-type EGFR gene and a RAS gene mutation were treated with escalating dose concentration of oridonin (from 2.5 to 50 µM). Antitumor effect was measured by 72-hr growth inhibition by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, and cell morphology was observed under microscope. Ongoing experiments will identify potential drug target(s) by assessing changes in global gene expression. Results: Oridonin exhibited a dose-dependent and time-dependent cytotoxic effect on a panel of NSCLC cell lines. Table 1 summarizes the molecular and histological features of these NSCLC cells, and their cytotoxicity to oridinin, erlotinib and pemetrexed. In those NSCLC cells that were sensitive to oridonin, morphological changes were consistent with autophagy and apoptosis. Potential drug targets will be verified by RT-PCR and immunoblotting. Conclusions: Oridonin exerts a distinct cytotoxicity that is independent of the sensitivity of NSCLC cells to erlotinib or pemetrexed. Further mechanistic and animal studies are warranted to understand its anti-tumor property and toxicity profile in preclinical evaluation. [Table: see text]


2020 ◽  
pp. 030089162096021
Author(s):  
Insha Bhat ◽  
Lawrence Okiror ◽  
Arjun Nair ◽  
Andrea Bille

Objective: There are limited data on tumour growth or pathologic upstaging in patients with early-stage lung cancer awaiting lung resection. We aimed to evaluate whether waiting times on the current lung cancer treatment pathway were associated with significant tumour growth or pathologic upstaging. Methods: This is a retrospective observational study of a consecutive series of patients with early-stage, non-small cell lung cancer who underwent resection for lung cancer. The difference between tumour size at diagnostic and preoperative computed tomography (CT) scans was calculated. Significant tumour growth was defined as a diameter increase of ⩾5 mm or ⩾20%. The time intervals between baseline and repeat CT (CT-int) and between baseline CT and date of surgery (Surg-int), as well as other potential clinical and pathologic prognostic factors, were compared between upstaged and nonupstaged patients. Results: There were 121 patients identified. Fifty-four patients (44.6%) had tumour growth ⩾5 mm and 27 patients (22%) had tumour growth ⩾20%. Median CT-int and Surg-int were 2.4 and 2.6 months, respectively. Forty-four patients (36%) were upstaged at surgery due to new lymph node involvement (n = 19), pleural invasion (n = 12), satellite nodules (n = 4), or increase in tumour diameter (n = 9). There was a marginal, but statistically insignificant, difference in median CT intervals in patients who had tumour growth <20% vs ⩾20% at 2.4 vs 2.6 months ( p = 0.06). Conclusion: Current cancer pathway waiting times are not associated with significant tumour growth or pathologic upstaging in this cohort.


2014 ◽  
Vol 99 (7) ◽  
pp. 974-984 ◽  
Author(s):  
Hui Xia ◽  
Yong-Fu Ma ◽  
Chang-Hai Yu ◽  
Ying-Jie Li ◽  
Jian Tang ◽  
...  

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