keyword
https://read.qxmd.com/read/38642413/targeting-cd8-t-cells-with-natural-products-for-tumor-therapy-revealing-insights-into-the-mechanisms
#21
REVIEW
Yuke Wang, Yan Zeng, Wenyong Yang, Xiuxuan Wang, Jingwen Jiang
BACKGROUND: Despite significant advances in cancer immunotherapy over the past decades, such as T cell-engaging chimeric antigen receptor (CAR)-T cell therapy and immune checkpoint blockade (ICB), therapeutic failure resulting from various factors remains prevalent. Therefore, developing combinational immunotherapeutic strategies is of great significance for improving the clinical outcome of cancer immunotherapy. Natural products are substances that naturally exist in various living organisms with multiple pharmacological or biological activities, and some of them have been found to have anti-tumor potential...
April 8, 2024: Phytomedicine
https://read.qxmd.com/read/38642371/discovery-and-mechanistic-studies-of-dual-target-hits-for-carbonic-anhydrase-ix-and-vegfr-2-as-potential-agents-for-solid-tumors-x-ray-in-vitro-in-vivo-and-in-silico-investigations-of-coumarin-based-thiazoles
#22
JOURNAL ARTICLE
Salma M Hefny, Tarek F El-Moselhy, Nabaweya El-Din, Simone Giovannuzzi, Thamer Bin Traiki, Mansoor-Ali Vaali-Mohammed, Ahmed M El-Dessouki, Koki Yamaguchi, Masaharu Sugiura, Moataz A Shaldam, Claudiu T Supuran, Maha-Hamadien Abdulla, Wagdy M Eldehna, Haytham O Tawfik
A dual-targeting approach is predicted to yield better cancer therapy outcomes. Consequently, a series of coumarin-based thiazoles ( 5a - h , 6 , and 7a - e ) were designed and constructed as potential carbonic anhydrase (CA) and VEGFR-2 suppressors. The inhibitory actions of the target compounds were assessed against CA isoforms IX and VEGFR-2. The assay results showed that coumarin-based thiazoles 5a , 5d , and 5e can effectively inhibit both targets. 5a , 5d , and 5e cytotoxic effects were tested on pancreatic, breast, and prostate cancer cells (PANC1, MCF7, and PC3)...
April 20, 2024: Journal of Medicinal Chemistry
https://read.qxmd.com/read/38642109/a-phase-i-trial-of-autologous-rak-cell-immunotherapy-in-metastatic-renal-cell-carcinoma
#23
JOURNAL ARTICLE
Jing Xu, Wen Zhang, Jinlian Tong, Caixia Liu, Qiaohui Zhang, Liren Cao, Jiangyong Yu, Aiping Zhou, Jie Ma
BACKGROUND: Treatment of metastatic renal cell carcinoma (mRCC) remains a challenge worldwide. Here, we introduced a phase I trial of autologous RAK cell therapy in patients with mRCC whose cancers progressed after prior systemic therapy. Although RAK cells have been used in clinic for many years, there has been no dose-escalation study to demonstrate its safety and efficacy. METHODS: We conducted a phase I trial with a 3 + 3 dose-escalation design to investigate the dose-related safety and efficacy of RAK cells in patients with mRCC whose cancers have failed to response to systemic therapy (ChiCTR1900021334)...
April 20, 2024: Cancer Immunology, Immunotherapy: CII
https://read.qxmd.com/read/38641734/single-cell-multiomic-dissection-of-response-and-resistance-to-chimeric-antigen-receptor-t-cells-against-bcma-in-relapsed-multiple-myeloma
#24
JOURNAL ARTICLE
Michael Rade, Nora Grieb, Ronald Weiss, Jaren Sia, Luise Fischer, Patrick Born, Andreas Boldt, Stephan Fricke, Paul Franz, Jonathan Scolnick, Lakshmi Venkatraman, Stacy Xu, Christina Kloetzer, Simone Heyn, Anne Sophie Kubasch, Ronny Baber, Song Yau Wang, Enrica Bach, Sandra Hoffmann, Jule Ussmann, Birthe Schetschorke, Saskia Hell, Sebastian Schwind, Klaus H Metzeler, Marco Herling, Madlen Jentzsch, Georg-Nikolaus Franke, Ulrich Sack, Ulrike Köhl, Uwe Platzbecker, Kristin Reiche, Vladan Vucinic, Maximilian Merz
Markers that predict response and resistance to chimeric antigen receptor (CAR) T cells in relapsed/refractory multiple myeloma are currently missing. We subjected mononuclear cells isolated from peripheral blood and bone marrow before and after the application of approved B cell maturation antigen-directed CAR T cells to single-cell multiomic analyses to identify markers associated with resistance and early relapse. Differences between responders and nonresponders were identified at the time of leukapheresis...
April 19, 2024: Nature Cancer
https://read.qxmd.com/read/38641541/prognostic-significance-of-immune-cell-infiltration-in-muscle-invasive-bladder-cancer-treated-with-definitive-chemoradiation-a-secondary-analysis-of-rtog-0524-and-rtog-0712
#25
JOURNAL ARTICLE
Zaker Rana, Sophia C Kamran, Amol C Shetty, Philip Sutera, Yang Song, Soha Bazyar, Abhishek A Solanki, Jeffry P Simko, Alan Pollack, David McConkey, Max Kates, M Minhaj Siddiqui, Jeffrey Hiken, Jon Earls, David Messina, Kent W Mouw, David Miyamoto, William U Shipley, M Dror Michaelson, Anthony Zietman, John J Coen, Douglas M Dahl, Ashesh B Jani, Luis Souhami, Brian K Chang, R Jeffrey Lee, Huong Pham, David T Marshall, Xinglei Shen, Stephanie L Pugh, Felix Y Feng, Jason A Efstathiou, Phuoc T Tran, Matthew P Deek
Chemoradiation therapy (CRT) is a treatment for muscle-invasive bladder cancer (MIBC). Using a novel transcriptomic profiling panel, we validated prognostic immune biomarkers to CRT using 70 pretreatment tumor samples from prospective trials of MIBC (NRG/RTOG 0524 and 0712). Disease-free survival (DFS) and overall survival (OS) were estimated via the Kaplan-Meier method and stratified by genes correlated with immune cell activation. Cox proportional-hazards models were used to assess group differences. Clustering of gene expression profiles revealed that the cluster with high immune cell content was associated with longer DFS (hazard ratio [HR] 0...
April 18, 2024: European Urology Oncology
https://read.qxmd.com/read/38641183/lymph-node-targeting-strategy-using-a-hydrogel-sustained-release-system-to-load-effector-memory-t-cells-improves-the-anti-tumor-efficacy-of-anti-pd-1
#26
JOURNAL ARTICLE
Hao Cui, Yu-Yue Zhao, Yan-Hua Han, Zhou Lan, Ke-Long Zou, Guo-Wang Cheng, Hao Chen, Pei-Liang Zhong, Yan Chen, Li-Min Ma, Tong-Kai Chen, Guang-Tao Yu
Communication between tumors and lymph nodes carries substantial significance for antitumor immunotherapy. Remodeling the immune microenvironment of tumor-draining lymph nodes (TdLN) plays a key role in enhancing the anti-tumor ability of immunotherapy. In this study, we constructed a biomimetic artificial lymph node structure composed of F127 hydrogel loading effector memory T (TEM ) cells and PD-1 inhibitors (aPD-1). The biomimetic lymph nodes facilitate the delivery of TEM cells and aPD-1 to the TdLN and the tumor immune microenvironment, thus realizing effective and sustained anti-tumor immunotherapy...
April 17, 2024: Acta Biomaterialia
https://read.qxmd.com/read/38641057/economic-evaluations-of-car-t-cell-therapies-for-hematologic-and-solid-malignancies-a-systematic-review
#27
REVIEW
Kednapa Thavorn, Emily Thompson, Srishti Kumar, Aliisa Heiskanen, Anubhav Agarwal, Harold Atkins, Risa Shorr, Terry Hawrysh, Kelvin Kar-Wing Chan, Justin Presseau, Daniel A Ollendorf, Ian D Graham, Jeremy M Grimshaw, Manoj Mathew Lalu, Surapon Nochaiwong, Dean A Fergusson, Brian Hutton, Doug Coyle, Natasha Kekre
OBJECTIVES: This study aims to systematically review evidence on the cost-effectiveness of chimeric antigen receptor (CAR)-T therapies for patients with cancer. METHODS: Electronic databases were searched in October 2022 and updated in September 2023. Systematic reviews, health technology assessments and economic evaluations that compared costs and effects of CAR-T therapy in cancer patients were included. Two reviewers independently screened studies, extracted data, synthesized results, and critically appraised studies using the Philips checklist...
April 17, 2024: Value in Health: the Journal of the International Society for Pharmacoeconomics and Outcomes Research
https://read.qxmd.com/read/38640784/implantable-car-t-cell-factories-enhance-solid-tumor-treatment
#28
JOURNAL ARTICLE
Sharda Pandit, Pritha Agarwalla, Feifei Song, Anton Jansson, Gianpietro Dotti, Yevgeny Brudno
Chimeric Antigen Receptor (CAR) T cell therapy has produced revolutionary success in hematological cancers such as leukemia and lymphoma. Nonetheless, its translation to solid tumors faces challenges due to manufacturing complexities, short-lived in vivo persistence, and transient therapeutic impact. We introduce 'Drydux' - an innovative macroporous biomaterial scaffold designed for rapid, efficient in-situ generation of tumor-specific CAR T cells. Drydux expedites CAR T cell preparation with a mere three-day turnaround from patient blood collection, presenting a cost-effective, streamlined alternative to conventional methodologies...
April 15, 2024: Biomaterials
https://read.qxmd.com/read/38640714/prospects-and-challenges-of-car-t-in-the-treatment-of-ovarian-cancer
#29
REVIEW
Biqing Chen, Jiaqi Liu
Ovarian cancer ranks as the seventh most prevalent cancer among women and is considered the most lethal gynecological malignancy on a global scale. The absence of reliable screening techniques, coupled with the insidious onset of nonspecific symptoms, often results in a delayed diagnosis, typically at an advanced stage characterized by peritoneal involvement. Management of advanced tumors typically involves a combination of chemotherapy and cytoreductive surgery. However, the therapeutic arsenal for ovarian cancer patients remains limited, highlighting the unmet need for precise, targeted, and sustained-release pharmacological agents...
April 18, 2024: International Immunopharmacology
https://read.qxmd.com/read/38639726/dual-responsive-nanomedicine-activates-programmed-antitumor-immunity-through-targeting-lymphatic-system
#30
JOURNAL ARTICLE
Hong Xiao, Xiaoxia Li, Simin Liang, Shuguang Yang, Shisong Han, Jinsheng Huang, Xintao Shuai, Jie Ren
Effective antitumor immunotherapy depends on evoking a cascade of cancer-immune cycles with lymph nodes (LNs) as the initial sites for activating antitumor immunity, making drug administration through the lymphatic system highly attractive. Here, we describe a nanomedicine with dual responsiveness to pH and enzyme for a programmed activation of antitumor immune through the lymphatic system. The proposed nanomedicine can release the STING agonist diABZI-C2-NH2 in the LNs' acidic environment to activate dendritic cells (DCs) and T cells...
April 19, 2024: ACS Nano
https://read.qxmd.com/read/38639669/synthetic-biology-approaches-for-enhancing-safety-and-specificity-of-car-t-cell-therapies-for-solid-cancers
#31
JOURNAL ARTICLE
Grace C Russell, Yassin Hamzaoui, Daniel Rho, Gaurav Sutrave, Joseph S Choi, Dara S Missan, Gabrielle A Reckard, Michael P Gustafson, Gloria B Kim
CAR-T cell therapies have been successful in treating numerous hematologic malignancies as the T cell can be engineered to target a specific antigen associated with the disease. However, translating CAR-T cell therapies for solid cancers is proving more challenging due to the lack of truly tumor-associated antigens and the high risk of off-target toxicities. To combat this, numerous synthetic biology mechanisms are being incorporated to create safer and more specific CAR-T cells that can be spatiotemporally controlled with increased precision...
March 30, 2024: Cytotherapy
https://read.qxmd.com/read/38639631/identification-of-the-immune-related-lncrna-snhg14-mir-200a-3p-pcolce2-axis-in-colorectal-cancer
#32
JOURNAL ARTICLE
Na Li, Jiangli Shen, Ximin Qiao, Qiang Liu, Xiaoqiang Dai, Xiongwen Jiao
CONTEXT: Procollagen C-endopeptidase enhancer 2 (PCOLCE2) is associated with the degradation of the extracellular matrix and collagen-chain trimerization, playing a yet unexplored role in tumor prognosis. OBJECTIVE: The study intended to characterize PCOLCE2's influence on colorectal cancer (CRC) using expression analysis and to investigate its prognostic potential. DESIGN: The research team performed a genetic analysis using genetic databases, including The Cancer Genome Atlas (TCGA), Gene Expression Profiling Interactive Analysis (GEPIA), the Tumor IMmune Estimation Resource (TIMER), and LinkedOmics...
April 18, 2024: Alternative Therapies in Health and Medicine
https://read.qxmd.com/read/38638445/phenotypic-immune-characterization-of-gastric-and-esophageal-adenocarcinomas-reveals-profound-immune-suppression-in-esophageal-tumor-locations
#33
JOURNAL ARTICLE
Tessa S Groen-van Schooten, Micaela Harrasser, Jens Seidel, Emma N Bos, Tania Fleitas, Monique van Mourik, Roos E Pouw, Ruben S A Goedegebuure, Benthe H Doeve, Jasper Sanders, Joris Bos, Mark I van Berge Henegouwen, Victor L J L Thijssen, Nicole C T van Grieken, Hanneke W M van Laarhoven, Tanja D de Gruijl, Sarah Derks
BACKGROUND: Tumors in the distal esophagus (EAC), gastro-esophageal junction including cardia (GEJAC), and stomach (GAC) develop in close proximity and show strong similarities on a molecular and cellular level. However, recent clinical data showed that the effectiveness of chemo-immunotherapy is limited to a subset of GEAC patients and that EACs and GEJACs generally benefit less from checkpoint inhibition compared to GACs. As the composition of the tumor immune microenvironment drives response to (immuno)therapy we here performed a detailed immune analysis of a large series of GEACs to facilitate the development of a more individualized immunomodulatory strategy...
2024: Frontiers in Immunology
https://read.qxmd.com/read/38638442/advancements-in-cancer-immunotherapies-targeting-cd20-from-pioneering-monoclonal-antibodies-to-chimeric-antigen-receptor-modified-t-cells
#34
REVIEW
Agnieszka Dabkowska, Krzysztof Domka, Malgorzata Firczuk
CD20 located predominantly on the B cells plays a crucial role in their development, differentiation, and activation, and serves as a key therapeutic target for the treatment of B-cell malignancies. The breakthrough of monoclonal antibodies directed against CD20, notably exemplified by rituximab, revolutionized the prognosis of B-cell malignancies. Rituximab, approved across various hematological malignancies, marked a paradigm shift in cancer treatment. In the current landscape, immunotherapies targeting CD20 continue to evolve rapidly...
2024: Frontiers in Immunology
https://read.qxmd.com/read/38638431/therapeutic-potential-of-interleukin-21-in-cancer
#35
REVIEW
Gheorghita Isvoranu, Marioara Chiritoiu-Butnaru
Interleukin-21 (IL-21) is an immunostimulatory cytokine which belongs to the common gamma-chain family of cytokines. It plays an import role in the development, differentiation, proliferation, and activation of immune cells, in particular T and natural killer (NK) cells. Since its discovery in 2000, IL-21 has been shown to regulate both adaptive and immune responses associates with key role in antiviral and antitumor responses. Recent advances indicate IL-21 as a promising target for cancer treatment and encouraging results were obtained in preclinical studies which investigated the potency of IL-21 alone or in combination with other therapies, including monoclonal antibodies, checkpoint inhibitory molecules, oncolytic virotherapy, and adoptive cell transfer...
2024: Frontiers in Immunology
https://read.qxmd.com/read/38638426/a-novel-dual-mechanism-of-action-bispecific-pd-1-il-2v-armed-by-a-%C3%AE-%C3%AE-only-interleukin-2-variant
#36
JOURNAL ARTICLE
Yongji Jiang, Chuyuan Chen, Yuan Liu, Rong Wang, Chuan Feng, Lili Cai, Shuang Chang, Lei Zhao
INTRODUCTION: Interleukin-2 (IL-2) is one of the first cytokines to be discovered as an immune agonist for cancer immunotherapy. Biased IL-2 variants had been discovered to eliminate Treg activation or enhance the tumor specific T cell cytotoxicity. However, all the biased IL-2 variants pose the risk to overstimulate immune response at a low-dose range. Here, we introduce a novel dual-MOA bispecific PD-1-IL-2v molecule with great anti-tumor efficacy in a high dosed manner. METHODS: The novel IL-2 variant was designed by structural truncation and shuffling...
2024: Frontiers in Immunology
https://read.qxmd.com/read/38638377/treatment-options-for-hepatocellular-carcinoma-using-immunotherapy-present-and-future
#37
REVIEW
Hongbin Wei, Chunlu Dong, Xun Li
Hepatocellular carcinoma (HCC) is a common cancer, and the body's immune responses greatly affect its progression and the prognosis of patients. Immunological suppression and the maintenance of self-tolerance in the tumor microenvironment are essential responses, and these form part of the theoretical foundations of immunotherapy. In this review, we first discuss the tumor microenvironment of HCC, describe immunosuppression in HCC, and review the major biomarkers used to track HCC progression and response to treatment...
April 28, 2024: Journal of Clinical and Translational Hepatology
https://read.qxmd.com/read/38638055/efficacy-and-biomarker-analysis-of-second-line-nab-paclitaxel-plus-sintilimab-in-patients-with-advanced-biliary-tract-cancer
#38
JOURNAL ARTICLE
Xiaofen Li, Nan Zhou, Yu Yang, Zijian Lu, Hongfeng Gou
Biliary tract cancer (BTC) is a highly aggressive malignancy with limited second-line therapy. We conducted this phase 2 trial to evaluate the efficacy and safety of second-line nab-paclitaxel plus sintilimab in advanced BTC. Histologically confirmed advanced BTC patients with documented disease progression after first-line chemotherapy were enrolled. Subjects received nab-paclitaxel 125 mg/m2 on days 1 and 8 plus sintilimab 200 mg on day 1, administered every 3 weeks. The primary end point was the objective response rate (ORR)...
April 18, 2024: Cancer Science
https://read.qxmd.com/read/38638035/optimizing-the-design-and-geometry-of-t-cell-engaging-bispecific-antibodies-targeting-cea-in-colorectal-cancer
#39
JOURNAL ARTICLE
Abdullah Elsayed, Louis Plüss, Larissa Nideroest, Giulia Rotta, Marina Thoma, Nathan Zangger, Frederik Peissert, Stefanie K Pfister, Christian Pellegrino, Sheila Dakhel Plaza, Roberto De Luca, Markus G Manz, Annette Oxenius, Emanuele Puca, Cornelia Halin, Dario Neri
Metastatic colorectal cancer (mCRC) remains a leading cause of cancer-related deaths, with a 5-year survival rate of only 15%. T cell engaging bispecific antibodies (TCBs) represent a class of biopharmaceuticals that redirect cytotoxic T cells towards tumor cells, thereby turning immunologically "cold" tumors "hot." The carcinoembryonic antigen (CEA) is an attractive tumor-associated antigen (TAA) that is overexpressed in over 98% of CRC patients. In this study, we report the comparison of four different TCB formats employing the antibodies F4 (targeting human CEA) and 2C11 (targeting mouse CD3ε)...
April 18, 2024: Molecular Cancer Therapeutics
https://read.qxmd.com/read/38637990/bis-2-f-cg-s-a-s-mp-isomers-encapsulated-in-cytidinyl-cationic-lipids-act-as-potent-in-situ-autologous-tumor-vaccines
#40
JOURNAL ARTICLE
Jing Yu, Xiaotong Yu, Xudong Sun, Quanxin Wang, Sijie Long, Runan Ren, Zhu Guan, Zhenjun Yang
Cancer immunotherapy has greatly improved the prognosis of tumor-bearing patients. Nevertheless, cancer patients exhibit low response rates to current immunotherapy drugs, such as PD1 and PDL1 antibodies. Cyclic dinucleotide analogs are a promising class of immunotherapeutic agents. In this study, in situ autologous tumor vaccines, composed of Bis-2'-F-cGS AS MP phosphonothioate isomers (FGA-di-pS-2 or FGA-di-pS-4) and cytidinyl/cationic lipids (Mix), were constructed. Intravenous (i.v.) and intratumoral (i...
April 17, 2024: Molecular Therapy
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