Current status and prospects of clinical treatment of osteosarcoma
ZY Jiang, JB Liu, XF Wang, YS Ma… - Technology in cancer …, 2022 - journals.sagepub.com
Osteosarcoma, one of the common malignant tumors in the skeletal system, originates in
mesenchymal tissue, and the most susceptible area of occurrence is the metaphysis with its …
mesenchymal tissue, and the most susceptible area of occurrence is the metaphysis with its …
Cancer cell cycle dystopia: heterogeneity, plasticity, and therapy
AK Witkiewicz, V Kumarasamy, I Sanidas, ES Knudsen - Trends in cancer, 2022 - cell.com
The mammalian cell cycle has been extensively studied regarding cancer etiology,
progression, and therapeutic intervention. The canonical cell cycle framework is supported …
progression, and therapeutic intervention. The canonical cell cycle framework is supported …
[HTML][HTML] An overview of resistance to chemotherapy in osteosarcoma and future perspectives
DY Garcia-Ortega, SA Cabrera-Nieto… - Cancer drug …, 2022 - ncbi.nlm.nih.gov
Osteosarcoma (OS) is the most common type of bone sarcoma. Despite the availability of
multimodal treatment with surgery and chemotherapy, the clinical results remain …
multimodal treatment with surgery and chemotherapy, the clinical results remain …
Clinical Targeted Next-Generation Panel Sequencing Reveals MYC Amplification Is a Poor Prognostic Factor in Osteosarcoma
PURPOSE Osteosarcoma risk stratification, on the basis of the presence of metastatic
disease at diagnosis and histologic response to chemotherapy, has remained unchanged …
disease at diagnosis and histologic response to chemotherapy, has remained unchanged …
[HTML][HTML] Signalling inhibition by ponatinib disrupts productive alternative lengthening of telomeres (ALT)
Alternative lengthening of telomeres (ALT) supports telomere maintenance in 10–15% of
cancers, thus representing a compelling target for therapy. By performing anti-cancer …
cancers, thus representing a compelling target for therapy. By performing anti-cancer …
[HTML][HTML] Mutant RB1 enhances therapeutic efficacy of PARPis in lung adenocarcinoma by triggering the cGAS/STING pathway
Q Dong, T Yu, B Chen, M Liu, X Sun, H Cao, K Liu… - JCI insight, 2023 - ncbi.nlm.nih.gov
Poly (ADP-ribose) polymerase inhibitors (PARPis) are approved for cancer therapy
according to their synthetic lethal interactions, and clinical trials have been applied in non …
according to their synthetic lethal interactions, and clinical trials have been applied in non …
[HTML][HTML] Identification of New Potential Prognostic and Predictive Markers in High-Grade Osteosarcoma Using Whole Exome Sequencing
R Gaeta, M Morelli, F Lessi, CM Mazzanti… - International journal of …, 2023 - mdpi.com
Conventional high-grade osteosarcoma (OS) is the most common primary cancer of bone
and it typically affects the extremities of adolescents. OS has a complex karyotype, and …
and it typically affects the extremities of adolescents. OS has a complex karyotype, and …
RB loss sensitizes cells to replication-associated DNA damage after PARP inhibition by trapping
LG Zamalloa, MM Pruitt, NM Hermance… - Life Science …, 2023 - life-science-alliance.org
The retinoblastoma tumor suppressor protein (RB) interacts physically and functionally with
a number of epigenetic modifying enzymes to control transcriptional regulation, respond to …
a number of epigenetic modifying enzymes to control transcriptional regulation, respond to …
[HTML][HTML] Molecularly Stratified Treatment Options in Primary Refractory DLBCL/HGBL with MYC and BCL2 or BCL6 Rearrangements (HGBL, NOS with MYC/BCL6)
HM Witte, J Riedl, A Künstner, A Fähnrich, J Ketzer… - Targeted Oncology, 2023 - Springer
Background There is growing evidence supporting multidisciplinary molecular tumor boards
(MTB) in solid tumors whereas hematologic malignancies remain underrepresented in this …
(MTB) in solid tumors whereas hematologic malignancies remain underrepresented in this …
[HTML][HTML] Contribution of microhomology to genome instability: connection between DNA repair and replication stress
Y Jiang - International Journal of Molecular Sciences, 2022 - mdpi.com
Microhomology-mediated end joining (MMEJ) is a highly mutagenic pathway to repair
double-strand breaks (DSBs). MMEJ was thought to be a backup pathway of homologous …
double-strand breaks (DSBs). MMEJ was thought to be a backup pathway of homologous …