A clinical evaluation of an ex vivo organ culture system to predict patient response to cancer therapy DOI Creative Commons
Shay Golan, Vered Bar, Seth J. Salpeter

и другие.

Frontiers in Medicine, Год журнала: 2023, Номер 10

Опубликована: Сен. 28, 2023

Ex vivo organ cultures (EVOC) were recently optimized to sustain cancer tissue for 5 days with its complete microenvironment. We examined the ability of an EVOC platform predict patient response therapy.A multicenter, prospective, single-arm observational trial. Samples obtained from patients newly diagnosed bladder who underwent transurethral resection tumor and core needle biopsies metastatic cancer. The tumors cut into 250 μM slices cultured within 24 h, then incubated 96 h vehicle or intended treat drug. fixed stained analyze their morphology cell viability. Each was given a score based on viability, level damage, Ki67 proliferation, scores correlated patients' clinical assessed by pathology Response Evaluation Criteria in Solid Tumors (RECIST).The microenvironment, including endothelial immune cells, preserved at high viability continued division days, demonstrating active signaling dynamics. A total 34 samples tested results. higher better response. system showed predictive specificity 77.7% (7/9, 95% CI 0.4-0.97) sensitivity 96% (24/25, 0.80-0.99).EVOC predicting therapy among muscle-invasive other solid tumors.

Язык: Английский

HER4 Affects Sensitivity to Tamoxifen and Abemaciclib in Luminal Breast Cancer Cells and Restricts Tumor Growth in MCF-7-Based Humanized Tumor Mice DOI Open Access

Veruschka Albert,

Christina Bruß,

Deniz Tümen

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(13), С. 7475 - 7475

Опубликована: Июль 8, 2024

The impact of the HER4 receptor on growth and treatment estrogen receptor-positive breast cancer is widely uncertain. Using CRISPR/Cas9 technology, we generated stable knockout variants derived from HER4-positive MCF-7, T-47D, ZR-75-1 cell lines. We investigated tumor proliferation as well cellular molecular mechanisms tamoxifen, abemaciclib, AMG232, NRG1 treatments a function in vitro. differentially affects response to tamoxifen abemaciclib treatment. Most conspicuous increased sensitivity MCF-7 vitro upon inhibition by NRG1. Additionally, assessed immunological effects responses therapy humanized mice (HTM) based HER4-wildtype corresponding HER4-knockout cells. Without any treatment, enhanced HTM suggests tumor-suppressive effect under preclinical but human-like conditions. This phenomenon associated with an HER2 expression vivo. Independent HER4, considerably inhibited these mice. However, abemaciclib-treated hormone patients tumor-associated mdm2 gene copy gains or pronounced showed reduced event-free survival. Evidently, presence efficacy different cells, even extents, unfavorable outcomes patients.

Язык: Английский

Процитировано

1

Interpretation of the past, present, and future of organoid technology: an updated bibliometric analysis from 2009 to 2024 DOI Creative Commons

Baozhen Qu,

Qiang Mu,

Huanhuan Bi

и другие.

Frontiers in Cell and Developmental Biology, Год журнала: 2024, Номер 12

Опубликована: Авг. 13, 2024

Organoid technology has been developed rapidly in the past decade, which involves exploration of mechanism development, regeneration and various diseases, intersects among multiple disciplines. Thousands literature on 3D-culture or organoids have published research areas cell biology tissue engineering, nanoscience, oncology so on, resulting it being challenging for researchers to timely summarize these studies. Bibliometric statistics is a helpful way help clarify above issues efficiently manage whole landscape systematically. In our study, all original articles were included Web Science database from January 2009 May 2024, related information was collected analyzed using Excel software, “bibliometrix” packages R VOSviewer CiteSpace. As results, total 6222 papers classify status quo predict future areas. Our findings highlight growing trend publications organoids, with United States Netherlands leading this field. The University California System, Harvard University, Utrecht Medical Center emerged as pivotal contributors key authors field include Clevers, H, Beekman, JM Spence JR. results also revealed that hotspots trends mainly focused clinical treatment, drug screening, application materials technologies such “hydrogel” “microfluidic technology” organoids. Next, we had an in-depth interpretation development process organoid area, including emergence technology, translation bench bedsides, profiles most widely studied types technologies, emerging organoid-immune co-cultures trends. Furthermore, discussed pitfalls, challenges prospects technology. conclusion, study provides readers straightforward convenient access

Язык: Английский

Процитировано

1

Global cluster analysis and network visualization in organoids in cancer research: a scientometric mapping from 1991 to 2021 DOI Creative Commons

S.‐F. TAN,

Jiali Deng,

Haobin Deng

и другие.

Frontiers in Oncology, Год журнала: 2023, Номер 13

Опубликована: Сен. 15, 2023

In the last three decades, there has been a surge in research on cancer organoids using 3D culture technologies, which resulted development of physiological human models. This study aims to provide an overview global trends and frontiers organoids.A total 3189 publications from 1991 2021 were collected Science Citation Index-Expanded (SCIE) Web (WoS). Bibliometric methods such as R package "Bibliometrix," Citespace, VOS viewer software employed investigate visualize bibliographic coupling, co-citation, co-authorship, co-occurrence trends, well publication field research.From 2021, significant increase organoids, with most articles being North America, Eastern Asia, Western Europe. The USA had highest number publications, citations, prolific authors, funding globally. Cancers was journal while Nature best link strength. Harvard University contributive institutions. this could be classified into five clusters: chemotherapy study, for drug screening, different models, molecular mechanism organoid construction. These areas are expected remain hotspots future research.The is based current trends.

Язык: Английский

Процитировано

3

Application and prospect of organoid technology in breast cancer DOI Creative Commons

S.Q. Huang,

Zifan Mei,

Andi Wan

и другие.

Frontiers in Immunology, Год журнала: 2024, Номер 15

Опубликована: Авг. 26, 2024

Breast cancer is the most common malignant tumor in women. Due to high heterogeneity of breast cells, traditional vitro research models still have major limitations. Therefore, it urgent establish an experimental model that can accurately simulate characteristics human cancer. organoid technology emerged as times required, is, construct tissue analogs with organ by using a patient’s through 3D culture . Since fully preserve histology and genetic original tumor, provides reliable for preclinical drug screening, establishment biobanks, into mechanisms development, determination targets. It has promoted personalized treatment clinical patients. This article mainly focuses on recent progress applications cancer, discussing current limitations prospects technology.

Язык: Английский

Процитировано

0

Targeting Myeloid Cells in Head and Neck Squamous Cell Carcinoma: A Kinase Inhibitor Library Screening Approach DOI Open Access
Mohamed Y. Zaky, Jessy John,

Monika Vashisht

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(22), С. 12277 - 12277

Опубликована: Ноя. 15, 2024

Head and neck squamous cell carcinoma (HNSCC) is highly enriched with tumor-infiltrating myeloid cells, including tumor-associated macrophages (TAMs) myeloid-derived suppressor cells (MDSCs). However, effective therapeutic agents targeting in HNSCC are currently lacking. Here, we employed a unique co-culture system to investigate how affect cells. We found that the presence of cancer significantly enhances proliferation promotes TAM differentiation. To identify potential agents, screened custom library 70 kinase inhibitors assess their effects on distinct subsets discovered specific differentially suppressed populations TAMs, monocytic MDSCs (M-MDSCs), or polymorphonuclear (PMN-MDSCs), suggesting inhibiting different targets could reduce Conversely, some were increase population CD11b+Ly6G−Ly6C− Among promising tested, vatalanib, VEGF-R inhibitor, demonstrated significant vivo efficacy at tumor growth reducing thereby underscoring its as agent. Our findings highlight differential modulatory HNSCC-associated caution application anti-cancer drugs. This experimental may provide robust platform for identifying new beyond, elucidating mechanistic insights into tumor-myeloid interaction.

Язык: Английский

Процитировано

0

Remodeling of tumour microenvironment: strategies to overcome therapeutic resistance and innovate immunoengineering in triple-negative breast cancer DOI Creative Commons
Desh Deepak Singh, Shafiul Haque, Youngsun Kim

и другие.

Frontiers in Immunology, Год журнала: 2024, Номер 15

Опубликована: Дек. 10, 2024

Triple-negative breast cancer (TNBC) stands as the most complex and daunting subtype of affecting women globally. Regrettably, treatment options for TNBC remain limited due to its clinical complexity. However, immunotherapy has emerged a promising avenue, showing success in developing effective therapies advanced cases improving patient outcomes. Improving treatments involves reducing side effects, minimizing systemic toxicity, enhancing efficacy. Unlike traditional immunotherapy, engineered nonmaterial's can precisely target TNBC, facilitating immune cell access, antigen presentation, triggering lasting responses. Nanocarriers with enhanced sensitivity specificity, specific cellular absorption, low toxicity are gaining attention. Nanotechnology-driven immunoengineering strategies focus on targeted delivery systems using multifunctional molecules precise tracking, diagnosis, therapy TNBC. This study delves into TNBC's tumour microenvironment (TME) remodeling, therapeutic resistance, nanotechnology.

Язык: Английский

Процитировано

0

Plasma-Activated Medium Inhibited the Proliferation and Migration of Non-Small Cell Lung Cancer A549 Cells in 3D Culture DOI Open Access

Zhidan Sun,

Chenglong Ding,

Yuhan Wang

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(24), С. 13262 - 13262

Опубликована: Дек. 10, 2024

Lung cancer is the most common type of malignant tumor worldwide. Plasma-activated medium (PAM) an innovative treatment method that has received considerable scientific attention. The objective this study to evaluate effects PAM on anti-tumor characteristics non-small cell lung (NSCLC) cells in two-dimensional (2D) and three-dimensional (3D) cultures. proliferative migratory capabilities A549 2D 3D cultures were assessed using MTT, migration, invasion assays, cycle, respectively. also investigated impact changes content intracellular extracellular reactive species analyzed protein expression Western Blot method. inhibited viability, abilities both cultures, suppressed epithelial–mesenchymal transition (EMT) process, downregulated RAS/ERK signaling pathway, which effectively spheroid formation. Additionally, effect was mediated through ROS-induced oxidative reactions, exhibited greater cytotoxicity culture compared culture. As 2D, model provides a viable vitro for studying mechanisms cancer. represents effective new NSCLC.

Язык: Английский

Процитировано

0

Mutant p53-Mediated Tumor Secretome: Bridging Tumor Cells and Stromal Cells DOI Open Access
Lei Qiu, Zelong Ma, Xiaoming Wu

и другие.

Genes, Год журнала: 2024, Номер 15(12), С. 1615 - 1615

Опубликована: Дек. 17, 2024

The tumor secretome comprises the totality of protein factors secreted by various cell components within microenvironment, serving as primary medium for signal transduction between cells and stromal cells. deletion or mutation p53 gene leads to alterations in cellular secretion characteristics, contributing construction microenvironment a non-autonomous manner. This review discusses critical roles mutant regulating remodel drive progression, influence plasticity cancer-associated fibroblasts (CAFs) well dynamics immunity focusing on both expression pathways. aim is provide new insights targeted cancer therapies.

Язык: Английский

Процитировано

0

A clinical evaluation of an ex vivo organ culture system to predict patient response to cancer therapy DOI Creative Commons
Shay Golan, Vered Bar, Seth J. Salpeter

и другие.

Frontiers in Medicine, Год журнала: 2023, Номер 10

Опубликована: Сен. 28, 2023

Ex vivo organ cultures (EVOC) were recently optimized to sustain cancer tissue for 5 days with its complete microenvironment. We examined the ability of an EVOC platform predict patient response therapy.A multicenter, prospective, single-arm observational trial. Samples obtained from patients newly diagnosed bladder who underwent transurethral resection tumor and core needle biopsies metastatic cancer. The tumors cut into 250 μM slices cultured within 24 h, then incubated 96 h vehicle or intended treat drug. fixed stained analyze their morphology cell viability. Each was given a score based on viability, level damage, Ki67 proliferation, scores correlated patients' clinical assessed by pathology Response Evaluation Criteria in Solid Tumors (RECIST).The microenvironment, including endothelial immune cells, preserved at high viability continued division days, demonstrating active signaling dynamics. A total 34 samples tested results. higher better response. system showed predictive specificity 77.7% (7/9, 95% CI 0.4-0.97) sensitivity 96% (24/25, 0.80-0.99).EVOC predicting therapy among muscle-invasive other solid tumors.

Язык: Английский

Процитировано

1