Conjugates of porphyrinoid-based photosensitizers with cytotoxic drugs: current progress and future directions toward selective photodynamic therapy

VF Otvagin, NS Kuzmina, ES Kudriashova… - Journal of medicinal …, 2022 - ACS Publications
Photodynamic therapy (PDT) is a treatment modality where light-mediated activation of
photosensitizers in a patient's body leads to the generation of cytotoxic reactive oxygen …

Lapatinib

M Voigtlaender, T Schneider-Merck… - Small molecules in …, 2018 - Springer
The human epidermal growth factor receptor (HER) family of receptor tyrosine kinases plays
an important role in the biology of many cancers. In breast and gastrointestinal cancer, and …

Covalent modifiers: A chemical perspective on the reactivity of α, β-unsaturated carbonyls with thiols via hetero-Michael addition reactions

PA Jackson, JC Widen, DA Harki… - Journal of medicinal …, 2017 - ACS Publications
Although Michael acceptors display a potent and broad spectrum of bioactivity, they have
largely been ignored in drug discovery because of their presumed indiscriminate reactivity …

[HTML][HTML] A novel STAT3 inhibitor W2014-S regresses human non-small cell lung cancer xenografts and sensitizes EGFR-TKI acquired resistance

Q Zheng, H Dong, J Mo, Y Zhang, J Huang… - Theranostics, 2021 - ncbi.nlm.nih.gov
Constitutive activation of signal transducer and activator of transcription 3 (STAT3) is a
common feature in human non-small cell lung cancer (NSCLC). STAT3 plays an important …

Discovery of (R,E)-N-(7-Chloro-1-(1-[4-(dimethylamino)but-2-enoyl]azepan-3-yl)-1H-benzo[d]imidazol-2-yl)-2-methylisonicotinamide (EGF816), a Novel, Potent …

G Lelais, R Epple, TH Marsilje, YO Long… - Journal of medicinal …, 2016 - ACS Publications
Over the past decade, first and second generation EGFR inhibitors have significantly
improved outcomes for lung cancer patients with activating mutations in EGFR. However …

Recent advances in covalent drug discovery

D Schaefer, X Cheng - Pharmaceuticals, 2023 - mdpi.com
In spite of the increasing number of biologics license applications, the development of
covalent inhibitors is still a growing field within drug discovery. The successful approval of …

[HTML][HTML] From mono-to bivalent: improving theranostic properties of target modules for redirection of UniCAR T cells against EGFR-expressing tumor cells in vitro and …

S Albert, C Arndt, S Koristka, N Berndt, R Bergmann… - Oncotarget, 2018 - ncbi.nlm.nih.gov
CAR-modified T cells show impressive results in clinical trials. However, cytokine release
syndrome and “on-target, off-tumor” reactions represent most concerning side effects. To …

The management of brain metastases in non-small cell lung cancer

S Owen, L Souhami - Frontiers in oncology, 2014 - frontiersin.org
Brain metastases (BM) are a common and lethal complication of non-small cell lung cancer
(NSCLC), which portend a poor prognosis. In addition, their management implies several …

Selumetinib overcomes gefitinib primary and acquired resistance by regulating MIG6/STAT3 in NSCLC

X Song, L Wang, W Tang, L Yuan, Q Liu, J Li… - Archives of Pharmacal …, 2023 - Springer
Gefitinib, as the first-generation epidermal growth factor receptor tyrosine kinase inhibitor
(EGFR-TKI), has achieved great advances in the treatment of non-small cell lung cancer …

[HTML][HTML] ALK-rearrangements and testing methods in non-small cell lung cancer: a review

RE Shackelford, M Vora, K Mayhall… - Genes & cancer, 2014 - ncbi.nlm.nih.gov
The anaplastic lymphoma tyrosine kinase (ALK) gene was first described as a driver
mutation in anaplastic non-Hodgkin's lymphoma. Dysregulated ALK expression is now an …