[HTML][HTML] KRAS mutation: from undruggable to druggable in cancer
L Huang, Z Guo, F Wang, L Fu - Signal transduction and targeted …, 2021 - nature.com
Cancer is the leading cause of death worldwide, and its treatment and outcomes have been
dramatically revolutionised by targeted therapies. As the most frequently mutated oncogene …
dramatically revolutionised by targeted therapies. As the most frequently mutated oncogene …
[HTML][HTML] Non-small-cell lung cancer in 2022: a review for general practitioners in oncology
H Mithoowani, M Febbraro - Current Oncology, 2022 - mdpi.com
Lung cancer is the leading cause of cancer death in Canada and a significant cause of
morbidity for patients and their loved ones. There have been rapid advances in preventing …
morbidity for patients and their loved ones. There have been rapid advances in preventing …
[HTML][HTML] Lineage tracing reveals the phylodynamics, plasticity, and paths of tumor evolution
Tumor evolution is driven by the progressive acquisition of genetic and epigenetic
alterations that enable uncontrolled growth and expansion to neighboring and distal tissues …
alterations that enable uncontrolled growth and expansion to neighboring and distal tissues …
[HTML][HTML] Uridine-derived ribose fuels glucose-restricted pancreatic cancer
Pancreatic ductal adenocarcinoma (PDA) is a lethal disease notoriously resistant to
therapy,. This is mediated in part by a complex tumour microenvironment, low vascularity …
therapy,. This is mediated in part by a complex tumour microenvironment, low vascularity …
NRF2 activation induces NADH-reductive stress, providing a metabolic vulnerability in lung cancer
Multiple cancers regulate oxidative stress by activating the transcription factor NRF2 through
mutation of its negative regulator, KEAP1. NRF2 has been studied extensively in KEAP1 …
mutation of its negative regulator, KEAP1. NRF2 has been studied extensively in KEAP1 …
Targeting oncogene and non-oncogene addiction to inflame the tumour microenvironment
Immune checkpoint inhibitors (ICIs) have revolutionized the clinical management of multiple
tumours. However, only a few patients respond to ICIs, which has generated considerable …
tumours. However, only a few patients respond to ICIs, which has generated considerable …
[HTML][HTML] Glutaminase inhibition impairs CD8 T cell activation in STK11-/Lkb1-deficient lung cancer
SA Best, PM Gubser, S Sethumadhavan, A Kersbergen… - Cell Metabolism, 2022 - cell.com
The tumor microenvironment (TME) contains a rich source of nutrients that sustains cell
growth and facilitate tumor development. Glucose and glutamine in the TME are essential for …
growth and facilitate tumor development. Glucose and glutamine in the TME are essential for …
O-GlcNAcylation promotes pancreatic tumor growth by regulating malate dehydrogenase 1
Q Zhu, H Zhou, L Wu, Z Lai, D Geng, W Yang… - Nature Chemical …, 2022 - nature.com
Oncogenic Kras-activated pancreatic ductal adenocarcinoma (PDAC) cells highly rely on an
unconventional glutamine catabolic pathway to sustain cell growth. However, little is known …
unconventional glutamine catabolic pathway to sustain cell growth. However, little is known …
[HTML][HTML] LncRNA FAM83A-AS1 facilitates tumor proliferation and the migration via the HIF-1α/glycolysis axis in lung adenocarcinoma
Z Chen, Z Hu, Q Sui, Y Huang, M Zhao… - … journal of biological …, 2022 - ncbi.nlm.nih.gov
Background: Lung adenocarcinoma (LUAD), the major subtype of lung cancer, is among the
leading cause of cancer-related death worldwide. Energy-related metabolic reprogramming …
leading cause of cancer-related death worldwide. Energy-related metabolic reprogramming …
Metabolic requirement for GOT2 in pancreatic cancer depends on environmental context
SA Kerk, L Lin, AL Myers, DJ Sutton, A Andren… - Elife, 2022 - elifesciences.org
Mitochondrial glutamate-oxaloacetate transaminase 2 (GOT2) is part of the malate-aspartate
shuttle, a mechanism by which cells transfer reducing equivalents from the cytosol to the …
shuttle, a mechanism by which cells transfer reducing equivalents from the cytosol to the …