keyword
https://read.qxmd.com/read/38654040/rapid-resistance-to-bet-inhibitors-is-mediated-by-fgfr1-in-glioblastoma
#41
JOURNAL ARTICLE
Anna M Jermakowicz, Alison M Kurimchak, Katherine J Johnson, Florence Bourgain-Guglielmetti, Simon Kaeppeli, Maurizio Affer, Hari Pradhyumnan, Robert K Suter, Winston Walters, Maria Cepero, James S Duncan, Nagi G Ayad
Bromodomain and extra-terminal domain (BET) proteins are therapeutic targets in several cancers including the most common malignant adult brain tumor glioblastoma (GBM). Multiple small molecule inhibitors of BET proteins have been utilized in preclinical and clinical studies. Unfortunately, BET inhibitors have not shown efficacy in clinical trials enrolling GBM patients. One possible reason for this may stem from resistance mechanisms that arise after prolonged treatment within a clinical setting. However, the mechanisms and timeframe of resistance to BET inhibitors in GBM is not known...
April 23, 2024: Scientific Reports
https://read.qxmd.com/read/38653965/targeting-nras-via-mir-1304-5p-or-farnesyltransferase-inhibition-confers-sensitivity-to-alk-inhibitors-in-alk-mutant-neuroblastoma
#42
JOURNAL ARTICLE
Perla Pucci, Liam C Lee, Miaojun Han, Jamie D Matthews, Leila Jahangiri, Michaela Schlederer, Eleanor Manners, Annabel Sorby-Adams, Joshua Kaggie, Ricky M Trigg, Christopher Steel, Lucy Hare, Emily R James, Nina Prokoph, Stephen P Ducray, Olaf Merkel, Firkret Rifatbegovic, Ji Luo, Sabine Taschner-Mandl, Lukas Kenner, G A Amos Burke, Suzanne D Turner
Targeting Anaplastic lymphoma kinase (ALK) is a promising therapeutic strategy for aberrant ALK-expressing malignancies including neuroblastoma, but resistance to ALK tyrosine kinase inhibitors (ALK TKI) is a distinct possibility necessitating drug combination therapeutic approaches. Using high-throughput, genome-wide CRISPR-Cas9 knockout screens, we identify miR-1304-5p loss as a desensitizer to ALK TKIs in aberrant ALK-expressing neuroblastoma; inhibition of miR-1304-5p decreases, while mimics of this miRNA increase the sensitivity of neuroblastoma cells to ALK TKIs...
April 23, 2024: Nature Communications
https://read.qxmd.com/read/38652971/targeting-siglec15-as-an-emerging-immunotherapy-for-anaplastic-thyroid-cancer
#43
JOURNAL ARTICLE
Lisha Bao, Ying Li, Xiaoping Hu, Yingying Gong, Jinming Chen, Ping Huang, Zhuo Tan, Minghua Ge, Zongfu Pan
Anaplastic thyroid carcinoma (ATC) is the most aggressive subtype of thyroid cancer with few effective therapies. Though immunotherapies such as targeting PD-1/PD-L1 axis have benefited patients with solid tumor, the druggable immune checkpoints are quite limited in ATC. In our study, we focused on the anti-tumor potential of sialic acid-binding Ig-like lectins (Siglecs) in ATC. Through screening by integrating microarray datasets including 216 thyroid-cancer tissues and single-cell RNA-sequencing, SIGLEC family members CD33, SIGLEC1, SIGLEC10 and SIGLEC15 were significantly overexpressed in ATC, among which SIGLEC15 increased highest and mainly expressed on cancer cells...
April 22, 2024: International Immunopharmacology
https://read.qxmd.com/read/38652658/multiplexed-single-cell-lineage-tracing-of-mitotic-kinesin-inhibitor-resistance-in-glioblastoma
#44
JOURNAL ARTICLE
Yim Ling Cheng, Matei A Banu, Wenting Zhao, Steven S Rosenfeld, Peter Canoll, Peter A Sims
Glioblastoma (GBM) is a deadly brain tumor, and the kinesin motor KIF11 is an attractive therapeutic target with roles in proliferation and invasion. Resistance to KIF11 inhibitors, which has mainly been studied in animal models, presents significant challenges. We use lineage-tracing barcodes and single-cell RNA sequencing to analyze resistance in patient-derived GBM neurospheres treated with ispinesib, a potent KIF11 inhibitor. Similar to GBM progression in patients, untreated cells lose their neural lineage identity and become mesenchymal, which is associated with poor prognosis...
April 21, 2024: Cell Reports
https://read.qxmd.com/read/38652539/mirna-148a-containing-gmsc-derived-evs-modulate-treg-th17-balance-via-ikkb-nf-%C3%AE%C2%BAb-pathway-and-treat-a-rheumatoid-arthritis-model
#45
JOURNAL ARTICLE
Jingrong Chen, Xiaoyi Shi, Yanan Deng, Junlong Dang, Yan Liu, Jun Zhao, Liang Rongzhen, Donglan Zeng, Wenbin Wu, Yiding Xiong, Jia Yuan, Ye Chen, Julie Wang, Weidong Lin, Xiangfang Chen, Weishan Huang, Nancy Olsen, Yunfeng Pan, Qing-Ling Fu, Song Guo Zheng
Mesenchymal stem cells (MSCs) have demonstrated potent immunomodulatory properties that have shown promise in the treatment of autoimmune diseases, including rheumatoid arthritis (RA). However, the inherent heterogeneity of MSCs triggered conflicting therapeutic outcomes, raising safety concerns and limiting their clinical application. This study aimed to investigate the potential of extracellular vesicles derived from human gingival mesenchymal stem cells (GMSC-EVs) as a therapeutic strategy for RA. Through in vivo experiments using an experimental RA model, our results demonstrated that GMSC-EVs selectively homed to inflamed joints and recovered Treg and Th17 cells balance, resulting in the reduction of arthritis progression...
April 23, 2024: JCI Insight
https://read.qxmd.com/read/38651826/mutant-ras-driven-secretome-causes-skeletal-muscle-defects-in-breast-cancer
#46
JOURNAL ARTICLE
Ruizhong Wang, Aditi S Khatpe, Brijesh Kumar, Henry Elmer Mang, Katie Batic, Adedeji K Adebayo, Harikrishna Nakshatri
Cancer-induced skeletal muscle defects differ in severity between individuals with the same cancer type. Cancer subtype-specific genomic aberrations are suggested to mediate these differences, but experimental validation studies are very limited. We utilized three different breast cancer patient-derived xenograft (PDX) models to correlate cancer subtype with skeletal muscle defects. PDXs were derived from brain metastasis of triple negative breast cancer (TNBC), Estrogen Receptor-positive/Progesterone Receptor-positive (ER+/PR+) primary breast cancer from a BRCA2-mutation carrier, and pleural effusion from an ER+/PR- breast cancer...
April 23, 2024: Cancer Res Commun
https://read.qxmd.com/read/38650011/znf692-promotes-osteosarcoma-cell-proliferation-migration-and-invasion-through-tnk2-mediated-activation-of-the-mek-erk-pathway
#47
JOURNAL ARTICLE
Di Zheng, Zhun Wei, Chong Zhang, Wenda Liu, Changtian Gong, Fei Wu, Weichun Guo
BACKGROUND: Osteosarcoma is a diverse and aggressive bone tumor. Driver genes regulating osteosarcoma initiation and progression remains incompletely defined. Zinc finger protein 692 (ZNF692), a kind of Krüppel C2H2 zinc finger transcription factor, exhibited abnormal expression in different types of malignancies and showed a correlation with the clinical prognosis of patients as well as the aggressive characteristics of cancer cells. Nevertheless, its specific role in osteosarcoma is still not well understood...
April 22, 2024: Biology Direct
https://read.qxmd.com/read/38650005/heterodimerization-of-t-cell-engaging-bispecific-antibodies-to-enhance-specificity-against-pancreatic-ductal-adenocarcinoma
#48
JOURNAL ARTICLE
Alan W Long, Hong Xu, Brian H Santich, Hongfen Guo, Sayed Shahabuddin Hoseini, Elisa de Stanchina, Nai-Kong V Cheung
BACKGROUND: EGFR and/or HER2 expression in pancreatic cancers is correlated with poor prognoses. We generated homodimeric (EGFRxEGFR or HER2xHER2) and heterodimeric (EGFRxHER2) T cell-engaging bispecific antibodies (T-BsAbs) to direct polyclonal T cells to these antigens on pancreatic tumors. METHODS: EGFR and HER2 T-BsAbs were constructed using the 2 + 2 IgG-[L]-scFv T-BsAbs format bearing two anti-CD3 scFvs attached to the light chains of an IgG to engage T cells while retaining bivalent binding to tumor antigens with both Fab arms...
April 23, 2024: Journal of Hematology & Oncology
https://read.qxmd.com/read/38649626/pdx-models-in-theranostic-applications-generation-and-screening-for-b-cell-lymphoma-of-human-origin
#49
JOURNAL ARTICLE
Shayla Shmuel, Sébastien Monette, Dina Ibrahim, Patrícia M R Pereira
This MIB guide briefly summarizes the generation of patient-derived xenografts (PDXs) and highlights the importance of validating PDX models for the presence of B cell lymphoma of human origin before their use in radiotheranostic applications. The use of this protocol will allow researchers to learn different methods for screening PDX models for Epstein-Barr virus (EBV)-infected B cell lymphoma.
April 22, 2024: Molecular Imaging and Biology: MIB: the Official Publication of the Academy of Molecular Imaging
https://read.qxmd.com/read/38647418/therapeutic-efficacy-of-ras-inhibitor-trametinib-using-a-juvenile-myelomonocytic-leukemia-patient-derived-xenograft-model
#50
JOURNAL ARTICLE
Alex Q Lee, Hiroaki Konishi, Masami Ijiri, Yueju Li, Arun Panigrahi, Jeremy Chien, Noriko Satake
Juvenile myelomonocytic leukemia (JMML) is an aggressive pediatric leukemia with few effective treatments and poor outcomes even after stem cell transplantation, the only current curative treatment. We developed a JMML patient-derived xenograft (PDX) mouse model and demonstrated the in vivo therapeutic efficacy and confirmed the target of trametinib, a RAS-RAF-MEK-ERK pathway inhibitor, in this model. A PDX model was created through transplantation of patient JMML cells into mice, up to the second generation, and successful engraftment was confirmed using flow cytometry...
April 22, 2024: Pediatric Hematology and Oncology
https://read.qxmd.com/read/38646856/correcting-mucogingival-deformities-for-pescatarian-patients-a-clinical-case-study
#51
Hyung Jae Jung, Nadeem Karimbux, Irina F Dragan
AIM: This clinical case study is to highlight the improvement of periodontal health of mandibular canines using a soft tissue alternative of fish origin, a piscine graft. METHODS: A 37-year-old female patient was referred to a periodontal practice for evaluation of mucogingival deformities around teeth #22 and #27 that were also diagnosed with recession, lack of keratinized tissue (KT), and bilateral high frenum attachment. Multiple soft tissue treatment options were presented to the patient, including autogenous, allograft, or xenograftporcine or piscine...
April 22, 2024: Clinical Advances in Periodontics
https://read.qxmd.com/read/38646654/the-hsp90-inhibitor-hvh-2930-exhibits-potent-efficacy-against-trastuzumab-resistant-her2-positive-breast-cancer
#52
JOURNAL ARTICLE
Minsu Park, Eunsun Jung, Jung Min Park, Soeun Park, Dongmi Ko, Juyeon Seo, Seongjae Kim, Kee Dal Nam, Yong Koo Kang, Lee Farrand, Van-Hai Hoang, Cong-Truong Nguyen, Minh Thanh La, Gibeom Nam, Hyun-Ju Park, Jihyae Ann, Jeewoo Lee, Yoon-Jae Kim, Ji Young Kim, Jae Hong Seo
Rationale: Resistance to targeted therapies like trastuzumab remains a critical challenge for HER2-positive breast cancer patients. Despite the progress of several N-terminal HSP90 inhibitors in clinical trials, none have achieved approval for clinical use, primarily due to issues such as induction of the heat shock response (HSR), off-target effects, and unfavorable toxicity profiles. We sought to examine the effects of HVH-2930, a novel C-terminal HSP90 inhibitor, in overcoming trastuzumab resistance. Methods: The effect of HVH-2930 on trastuzumab-sensitive and -resistant cell lines in vitro was evaluated in terms of cell viability, expression of HSP90 client proteins, and impact on cancer stem cells...
2024: Theranostics
https://read.qxmd.com/read/38646643/exploring-the-role-of-combined-external-beam-radiotherapy-and-targeted-radioligand-therapy-with-177-lu-lu-psma-617-for-prostate-cancer-from-bench-to-bedside
#53
JOURNAL ARTICLE
Daria Arbuznikova, Aikaterini Klotsotyra, Lisa Uhlmann, Lisa-Charlotte Domogalla, Nils Steinacker, Michael Mix, Gabriele Niedermann, Simon K B Spohn, Martin T Freitag, Anca L Grosu, Philipp T Meyer, Christian Gratzke, Matthias Eder, Constantinos Zamboglou, Ann-Christin Eder
Management of prostate cancer (PC) might be improved by combining external beam radiotherapy (EBRT) and prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (RLT) with lutetium-177 (177 Lu)-labeled PSMA inhibitors. We hypothesized a higher efficacy of the combination due to augmentation of the radiation dose to the tumor and interactions of EBRT with PSMA expression potentially increasing radiopharmaceutical uptake. Therefore, this study analyzed the influence of radiation on PSMA expression levels in vitro ...
2024: Theranostics
https://read.qxmd.com/read/38646155/phosphoproteomic-analysis-identified-mutual-phosphorylation-of-fak-and-src-as-a-mechanism-of-osimertinib-resistance-in-egfr-mutant-lung-cancer
#54
JOURNAL ARTICLE
Takehiro Tozuka, Rintaro Noro, Keisuke Yoshida, Satoshi Takahashi, Mariko Hirao, Kuniko Matsuda, Yasuhiro Kato, Shinji Nakamichi, Susumu Takeuchi, Masaru Matsumoto, Akihiko Miyanaga, Shinobu Kunugi, Kazufumi Honda, Jun Adachi, Masahiro Seike
INTRODUCTION: Osimertinib is a standard treatment for patients with EGFR -mutant NSCLC. Although some osimertinib resistance mechanisms have been identified, nearly 50% of the mechanisms remain to be elucidated. This study was aimed at identifying non-genetic mechanisms underlying osimertinib resistance. METHODS: We established two osimertinib-resistant cell lines from EGFR mutation-positive PC-9 and HCC827 NSCLC cell lines (PC-9OR and HCC827OR, respectively) using a stepwise method...
April 2024: JTO clinical and research reports
https://read.qxmd.com/read/38645554/surufatinib-combined-with-photodynamic-therapy-induces-ferroptosis-to-inhibit-cholangiocarcinoma-in-vitro-and-in-tumor-models
#55
JOURNAL ARTICLE
Yun-Peng Huang, Yong-Xiang Wang, Hui Zhou, Zhong-Tao Liu, Zi-Jian Zhang, Li Xiong, Heng Zou, Yu Wen
The curative effect of single therapy for advanced cholangiocarcinoma (CCA) is poor, thus investigating combined treatment strategies holds promise for improving prognosis. Surufatinib (SUR) is a novel multikinase inhibitor that has been confirmed to prolong survival of patients with advanced CCA. Photodynamic therapy (PDT) can also ablate advanced CCA and relieve biliary obstruction. In this study, we explored the anti-CCA effect of SUR combined with PDT, and explored the underlying mechanism. We found that SUR could effectively inhibit the abilities of proliferation, migration and metastasis in CCA cells (HUCCT-1, RBE)...
2024: Frontiers in Pharmacology
https://read.qxmd.com/read/38645113/nitric-oxide-inhibits-ten-eleven-translocation-dna-demethylases-to-regulate-5mc-and-5hmc-across-the-genome
#56
Douglas Thomas, Marianne Palczewski, Hannah Kuschman, Brian Hoffman, Hao Yang, Sharon Glynn, David Wilson, Eric Kool, William Montfort, Jenny Chang, Aydolun Petenkaya, Constantinos Chronis, Thomas Cundari, Sushma Sappa, Kabirul Islam, Daniel McVicar, Yu Fan, Qingrong Chen, Daoud Meerzaman, Michael Sierk
DNA methylation at cytosine bases of eukaryotic DNA (5-methylcytosine, 5mC) is a heritable epigenetic mark that can regulate gene expression in health and disease. Enzymes that metabolize 5mC have been well-characterized, yet the discovery of endogenously produced signaling molecules that regulate DNA methyl-modifying machinery have not been described. Herein, we report that the free radical signaling molecule nitric oxide (NO) can directly inhibit the Fe(II)/2-OG-dependent DNA demethylases ten-eleven translocation (TET) and human AlkB homolog 2 (ALKBH2)...
April 3, 2024: Research Square
https://read.qxmd.com/read/38644862/mir-199a-5p-targets-dusp14-to-regulate-cell-proliferation-invasion-and-stemness-in-non-small-cell-lung-cancer
#57
JOURNAL ARTICLE
Ying Zheng, Chaokun Yang, Shaoqiang Xie, Desheng Liu, Hui Wang, Jinxin Liu
BACKGROUND: Non-small cell lung cancer (NSCLC) shows the highest morbidity among malignant tumors worldwide. Despite improvements of diagnosis and treatment, patient prognosis remains unfavorable. Therefore, there is a need to discover a novel treatment strategy for NSCLC. DUSP14 is related to various cancers as the regulatory factor for cellular processes. However, its specific roles in NSCLC and the upstream modulator remain largely unclear. METHODS: DUSP14 expression patterns within the lung cancer patient cohort from TCGA database were analyzed using UALCAN online tool...
April 30, 2024: Heliyon
https://read.qxmd.com/read/38644551/usp19-regulates-dna-methylation-damage-repair-and-confers-temozolomide-resistance-through-mgmt-stabilization
#58
JOURNAL ARTICLE
Jiaqi Liu, Kaikai Wang, Qian Zhu, Yixin Zhang, Yuping Chen, Zhenkun Lou, Jian Yuan
OBJECTIVE: To elucidate the relationship between USP19 and O(6)-methylguanine-DNA methyltransferase (MGMT) after temozolomide treatment in glioblastoma (GBM) patients with chemotherapy resistance. METHODS: Screening the deubiquitinase pannel and identifying the deubiquitinase directly interacts with and deubiquitination MGMT. Deubiquitination assay to confirm USP19 deubiquitinates MGMT. The colony formation and tumor growth study in xenograft assess USP19 affects the GBM sensitive to TMZ was performed by T98G, LN18, U251, and U87 cell lines...
April 2024: CNS Neuroscience & Therapeutics
https://read.qxmd.com/read/38643278/bispecific-car-t-cell-therapy-targeting-bcma-and-cd19-in-relapsed-refractory-multiple-myeloma-a-phase-i-ii-trial
#59
JOURNAL ARTICLE
Ming Shi, Jiaojiao Wang, Hongming Huang, Dan Liu, Hai Cheng, Xu Wang, Wei Chen, Zhiling Yan, Wei Sang, Kunming Qi, Depeng Li, Feng Zhu, Zhenyu Li, Jianlin Qiao, Qingyun Wu, Lingyu Zeng, Xiaoming Fei, Weiying Gu, Yuqing Miao, Kailin Xu, Junnian Zheng, Jiang Cao
Despite the high therapeutic response achieved with B-cell maturation antigen (BCMA)-specific chimeric antigen receptor (CAR) T-cell therapy in relapsed and refractory multiple myeloma (R/R MM), primary resistance and relapse exist with single-target immunotherapy. Here, we design bispecific BC19 CAR T cells targeting BCMA/CD19 and evaluate antimyeloma activity in vitro and in vivo. Preclinical results indicate that BC19 CAR specifically recognize target antigens, and BC19 CAR T cells mediate selective killing of BCMA or CD19-positive cancer cells...
April 20, 2024: Nature Communications
https://read.qxmd.com/read/38641704/narazaciclib-a-novel-multi-kinase-inhibitor-with-potent-activity-against-csf1r-flt3-and-cdk6-shows-strong-anti-aml-activity-in-defined-preclinical-models
#60
JOURNAL ARTICLE
Tao Yang, Hang Ke, Jinping Liu, Xiaoyu An, Jia Xue, Jinying Ning, Feng Hao, Lingxin Xiong, Cen Chen, Yueying Wang, Jia Zheng, Bing Gao, Zhengzheng Bao, Kefeng Gong, Lei Zhang, Faming Zhang, Sheng Guo, Qi-Xiang Li
CSF1R is a receptor tyrosine kinase responsible for the growth/survival/polarization of macrophages and overexpressed in some AML patients. We hypothesized that a novel multi-kinase inhibitor (TKi), narazaciclib (HX301/ON123300), with high potency against CSF1R (IC50  ~ 0.285 nM), would have anti-AML effects. We tested this by confirming HX301's high potency against CSF1R (IC50  ~ 0.285 nM), as well as other kinases, e.g. FLT3 (IC50 of ~ 19.77 nM) and CDK6 (0...
April 19, 2024: Scientific Reports
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