Pleural empyema due to Salmonella in a patient with bronchogenic carcinoma: the first case report from a cancer hospital in Egypt

A Samir Abdelhafiz, M Wassef… - Access …, 2020 - microbiologyresearch.org
Background. Salmonella species are motile, Gram-negative facultative anaerobic bacilli,
which belong to the family Enterobacteriaceae. The most common clinical presentations of …

[HTML][HTML] Detection of microRNA-200b may predict the inhibitory effect of gefitinib on non‑small cell lung cancer and its potential mechanism

Z Liu, L Yao, B Tan, L Li, B Chen - Oncology Letters, 2016 - spandidos-publications.com
The present study aimed to investigate the association and underlying mechanisms
between microRNA-200b level and the inhibitory effect of gefitinib on non-small cell lung …

[HTML][HTML] 雷公藤甲素与吉非替尼序贯应用对人肺腺癌细胞H1975 存活及凋亡通路的影响

张鑫宇, 刘皈阳, 刘浩, 马涛 - Chinese Journal of Lung Cancer, 2015 - ncbi.nlm.nih.gov
背景与目的表皮生长因子受体(epidermal growth factor receptor, EGFR) 酪氨酸激酶抑制剂(
tyrosine kinase inhibitors, TKIs) 被用于治疗进展性晚期非小细胞肺癌(non-small cell lung …

A different approach to the EGFR inhibitor Gefitinib involving solid-phase synthesis

A Sequeira, A Lourenco, LM Ferreira, PS Branco… - Synlett, 2018 - thieme-connect.com
An efficient solid-phase synthesis approach is here reported for the first time to prepare the
EGFR inhibitor Gefitinib. The five-step synthetic strategy used FMP resin as the solid …

苦参碱抑制Nrf2 诱导的Annexin A4 表达改善非小细胞肺癌对顺铂耐药

刘冬, 周伟, 高晓博, 王小霞, 郭舜, 石磊, 张松 - 临床与病理杂志, 2019 - cqvip.com
目的: 探讨苦参碱对非小细胞肺癌(non-small lung cancer cell, NSCLC) 顺铂耐药性的逆转作用
及其机制. 方法: MTT 法检测细胞存活率; 采用试剂盒检测细胞乳酸脱氢酶及caspase-3 活性 …

The Role of Tyrosine Kinase Inhibitors in Reduction of Mortality from Non-small Cell Lung Cancer: A Meta-analysis

T Lian, X Zhang - Combinatorial Chemistry & High Throughput …, 2023 - ingentaconnect.com
Background: Tyrosine kinase inhibitors are widely used in the treatment of non-small cell
lung cancer. However, the exact role of these inhibitors, particularly in the reduction of …

Synthesis and Antiproliferative Activities of Novel Substituted 5‐Anilino‐α‐Glucofuranose Derivatives

Y Zhang, L Wang, B Sun, X Li, Q Hou… - Chemistry & …, 2020 - Wiley Online Library
In order to find novel antitumor candidate agents with high efficiency and low toxicity, 14
novel substituted 5‐anilino‐α‐glucofuranose derivatives have been designed, synthesized …

Design and synthesis of novel 6-substituted quinazoline-2-thiols

SK Pulakhandam, NK Katari, SB Jonnalagadda - Molecular Diversity, 2019 - Springer
A novel design and efficient protocol for the synthesis of new class of 6-substituted
quinazoline-2-thiols is reported. The derivatization of the thioquinazolines is achieved in a …

Design, Synthesis and Anticancer Properties of Novel Hydrazino-Fused Pyrimidines.

SK MITTAPALLI, I RIZWANA… - Oriental Journal of …, 2023 - search.ebscohost.com
Globally widespread cancer causes an urgent need to develop innovative, more potent
drugs that can deliver better therapeutic outcomes. The study aimed to synthesize pyazolo …

Development and characterization of oncolytic adenoviral vectors for the treatment of head and neck cancer

F Wienen - 2023 - oparu.uni-ulm.de
Human adenovirus type 5 (HAdV-5)-based oncolytic virotherapy holds promise as efficient
anti-cancer therapy. Beside a direct virus-induced cancer cell lysis, the resultant release of …