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Targeting mutant p53 for cancer therapy: direct and indirect strategies
J Hu, J Cao, W Topatana, S Juengpanich, S Li… - Journal of hematology & …, 2021 - Springer
TP53 is a critical tumor-suppressor gene that is mutated in more than half of all human
cancers. Mutations in TP53 not only impair its antitumor activity, but also confer mutant p53 …
cancers. Mutations in TP53 not only impair its antitumor activity, but also confer mutant p53 …
Hypoxia as a driver of resistance to immunotherapy
J Kopecka, IC Salaroglio, E Perez-Ruiz… - Drug Resistance …, 2021 - Elsevier
Hypoxia, a hallmark of solid tumors, determines the selection of invasive and aggressive
malignant clones displaying resistance to radiotherapy, conventional chemotherapy or …
malignant clones displaying resistance to radiotherapy, conventional chemotherapy or …
Evolutionary trajectories of small cell lung cancer under therapy
J George, L Maas, N Abedpour, M Cartolano, L Kaiser… - Nature, 2024 - nature.com
The evolutionary processes that underlie the marked sensitivity of small cell lung cancer
(SCLC) to chemotherapy and rapid relapse are unknown,–. Here we determined tumour …
(SCLC) to chemotherapy and rapid relapse are unknown,–. Here we determined tumour …
The gut microbiome switches mutant p53 from tumour-suppressive to oncogenic
E Kadosh, I Snir-Alkalay, A Venkatachalam, S May… - Nature, 2020 - nature.com
Somatic mutations in p53, which inactivate the tumour-suppressor function of p53 and often
confer oncogenic gain-of-function properties, are very common in cancer,. Here we studied …
confer oncogenic gain-of-function properties, are very common in cancer,. Here we studied …
Taxanes in cancer treatment: Activity, chemoresistance and its overcoming
Since 1984, when paclitaxel was approved by the FDA for the treatment of advanced
ovarian carcinoma, taxanes have been widely used as microtubule-targeting antitumor …
ovarian carcinoma, taxanes have been widely used as microtubule-targeting antitumor …
Schiff bases and their metal complexes to target and overcome (multidrug) resistance in cancer
Overcoming multidrug resistance (MDR) is one of the major challenges in cancer therapy. In
this respect, Schiff base-related compounds (bearing a R 1 R 2 Cdouble bondNR 3 bond) …
this respect, Schiff base-related compounds (bearing a R 1 R 2 Cdouble bondNR 3 bond) …
[HTML][HTML] Selenium and tellurium in the development of novel small molecules and nanoparticles as cancer multidrug resistance reversal agents
Selenium is an essential trace element that is crucial for cellular antioxidant defense against
reactive oxygen species (ROS). Recently, many selenium-containing compounds have …
reactive oxygen species (ROS). Recently, many selenium-containing compounds have …
Cell fate regulation governed by p53: Friends or reversible foes in cancer therapy
B Song, P Yang, S Zhang - Cancer communications, 2024 - Wiley Online Library
Cancer is a leading cause of death worldwide. Targeted therapies aimed at key oncogenic
driver mutations in combination with chemotherapy and radiotherapy as well as …
driver mutations in combination with chemotherapy and radiotherapy as well as …
Overcoming anti-cancer drug resistance via restoration of tumor suppressor gene function
The cytotoxic anti-cancer drugs cisplatin, paclitaxel, doxorubicin, 5-fluorouracil (5-FU), as
well as targeted drugs including imatinib, erlotinib, and nivolumab, play key roles in clinical …
well as targeted drugs including imatinib, erlotinib, and nivolumab, play key roles in clinical …
Surmounting cancer drug resistance: New insights from the perspective of N6-methyladenosine RNA modification
Despite the development of targeted therapy, drug resistance remains a primary hindrance
to curative treatment of various cancers. Among several novel approaches to overcome drug …
to curative treatment of various cancers. Among several novel approaches to overcome drug …