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  • Open Access

    ARTICLE

    Diverse PD-1, CD163, and FOXP3 Profiles in Primary and Metastatic Microenvironments of Prostate Cancer

    Ana Clara Ciglioni Salustiano1,2, Gabriela Barbosa1,3,4, Rodolfo Borges dos Reis2,4, Amílcar Castro de Mattos5,6, Athanase Billis6, Leonardo O. Reis1,3,4,*

    Oncology Research, Vol.33, No.11, pp. 3417-3428, 2025, DOI:10.32604/or.2025.068023 - 22 October 2025

    Abstract Objective: The tumor microenvironment plays a pivotal role in prostate cancer progression and may differ across metastatic sites. This study aimed to evaluate and compare the primary and metastatic prostate adenocarcinoma tumor microenvironment. Methods: A total of 27 formalin-fixed paraffin-embedded tissue samples derived from 17 patients diagnosed with prostate adenocarcinoma, including the primary tumors, and the corresponding metastatic lymphatic and hematogenous lesions from various anatomical sites. Immunohistochemical labeling was performed using antibodies against Cluster of Differentiation 3 epsilon chain (CD3e), CD8 alpha chain (CD8a), Cluster of Differentiation 68 (CD68), Cluster of Differentiation 163 (CD163), Forkhead… More > Graphic Abstract

    Diverse PD-1, CD163, and FOXP3 Profiles in Primary and Metastatic Microenvironments of Prostate Cancer

  • Open Access

    ARTICLE

    RAD23B Promotes Colorectal Cancer Metastasis via the Talin1/Integrin/PI3K/AKT/MMP9 Axis

    Jun Li1,#, Yang Chen1,#, Zhijiao Hao2, Zhiyong Zhang3, Jingyi Fan1, Xiao Liu1, Xueli Zhao3, Hongyan Zhang4, Chenpeng Wu3,*

    Oncology Research, Vol.33, No.11, pp. 3523-3541, 2025, DOI:10.32604/or.2025.067535 - 22 October 2025

    Abstract Background: Radiation sensitive 23 homolog B (RAD23B), a DNA repair-related protein, plays a contributory role in the development of multiple malignancies. This study aimed to explore the role of RAD23B in promoting colorectal cancer (CRC) metastasis and to elucidate the underlying molecular mechanisms. Methods: RAD23B was overexpressed in CRC cell lines SW480 and HCT-8, with empty vectors serving as controls. Invasion, cell proliferation, and migration were assessed using CCK-8 and Transwell assays. A xenograft mouse model was used to evaluate metastatic potential in vivo. Immunoprecipitation-mass spectrometry (IP-MS) and transcriptomic analysis by RNA sequencing (RNA-seq) were performed… More >

  • Open Access

    RETRACTION

    Retraction: Long Noncoding RNA SChLAP1 Accelerates the Proliferation and Metastasis of Prostate Cancer via Targeting miR-198 and Promoting the MAPK1 Pathway

    Oncology Research Editorial Office

    Oncology Research, Vol.33, No.10, pp. 3159-3159, 2025, DOI:10.32604/or.2025.073035 - 26 September 2025

    Abstract This article has no abstract. More >

  • Open Access

    ARTICLE

    3-Hydroxysterol Δ24-Reductase Promotes Ovarian Cancer Progression by Activating the TGF-1/Smad2/3 Signaling Pathway

    Wenjing Liao1,#, Liaodi Wang2,#, Zhen Huang1, Ziyu Zou1, Yimin Liu1, Haoyue Liu1, Zhaoning Duan1, Liangdan Tang1,*

    Oncology Research, Vol.33, No.10, pp. 3041-3064, 2025, DOI:10.32604/or.2025.065451 - 26 September 2025

    Abstract Objectives: Ovarian cancer (OC) is a highly heterogeneous disease characterized by high metastatic potential and frequent recurrence. 3β-hydroxysterol Δ24-reductase (DHCR24) is closely associated with the progression of various malignant tumors, but its role in OC remains unexplored. This study is the first to systematically investigate the function of DHCR24 in OC and elucidate its mechanism in promoting OC progression, providing novel theoretical insights for targeted therapy. Methods: The expression of DHCR24 was evaluated in tissues using bioinformatics and clinical data; the impact of DHCR24 on the malignant behavior of OC was assessed through in vivo and inMore >

  • Open Access

    CASE REPORT

    Tumor-to-tumor metastasis: case report of a neuroendocrine tumor of the lung metastasizing to a benign oncocytoma of the kidney

    Siddharth Marthi1,*, Muhammad Mukarram1, Fatemeh Ardeshir-Larijani2, Lara Rabih Harik3, Shreyas Subhash Joshi1,2

    Canadian Journal of Urology, Vol.32, No.4, pp. 349-353, 2025, DOI:10.32604/cju.2025.063775 - 29 August 2025

    Abstract Tumor-to-tumor metastasis (TTM) is a rare phenomenon in which a secondary tumor colonizes within a primary tumor of a different histogenesis. It is hypothesized that TTM is encouraged by conditions that promote increased cell growth and division in the primary tumor, such as hypervascularity and expression of oncogenic cytokines. However, the exact causes of TTM likely vary on a case-by-case basis and are dependent on the microenvironment of both the primary and secondary tumors. Herein, we present the first reported example of TTM in which a pulmonary neuroendocrine tumor (NET) metastasizes to a renal oncocytoma. More >

  • Open Access

    RETRACTION

    Retraction: UCA1 Regulates the Growth and Metastasis of Pancreatic Cancer by Sponging miR-135a

    Oncology Research Editorial Offfce

    Oncology Research, Vol.33, No.9, pp. 2597-2597, 2025, DOI:10.32604/or.2025.071883 - 28 August 2025

    Abstract This article has no abstract. More >

  • Open Access

    RETRACTION

    Retraction: Inhibition of Liver Carcinoma Cell Invasion and Metastasis by Knockdown of Cullin7 In Vitro and In Vivo

    Oncology Research Editorial Offfce

    Oncology Research, Vol.33, No.8, pp. 2179-2179, 2025, DOI:10.32604/or.2025.070134 - 18 July 2025

    Abstract This article has no abstract. More >

  • Open Access

    ARTICLE

    Intrathecal Pemetrexed Administration and Myelosuppression in Patients with Leptomeningeal Metastases from Lung Adenocarcinoma: A Retrospective Study

    Junxing Chen1,#, Luping Pan1,#, Yunzhi Liu1,2, Yan Fang1, Ruoxuan Li1, Zhiqin Lu1,3, Anwen Liu1,4, Yanqing He5,*, Zhimin Zeng1,6,*

    Oncology Research, Vol.33, No.8, pp. 2107-2121, 2025, DOI:10.32604/or.2025.064237 - 18 July 2025

    Abstract Background: Non-small cell lung cancer (NSCLC) patients with leptomeningeal metastasis (LM) have a very poor prognosis. Intrathecal pemetrexed (IP) has shown moderate efficacy in treating patients with NSCLC-LM. Myelosuppression is the most common adverse effect following IP administration. Despite this trend, the specific risk factors contributing to IP-related myelosuppression remain unclear. Methods: This study conducted a retrospective analysis of lung adenocarcinoma (LUAD) patients with LM who received IP treatment at the Second Affiliated Hospital of Nanchang University from April 2017 to April 2024. Risk factors for myelosuppression were identified through univariate and multivariate logistic regression… More >

  • Open Access

    ARTICLE

    Tumor-expressing PD-L1 regulates NT5E expression through MAPK/ERK pathway in triple-negative breast cancer

    CHENG CHENG1,2,3, CHAO SHI1,2, SHANG WU1,2, WEIXING WU3, JINGPING LI1,2, SINUO GAO1,2, MENG HAN3, YIMIN WANG3, XIANGMEI ZHANG2,4,*, YUNJIANG LIU1,2,*

    Oncology Research, Vol.33, No.7, pp. 1633-1648, 2025, DOI:10.32604/or.2025.061637 - 26 June 2025

    Abstract Objectives: While programmed cell death 1 (PD-1) inhibitors have improved cancer treatment, the function and mechanisms of programmed cell death ligand 1 (PD-L1), particularly when expressed by cancer cells, remain unclear. This study aims to explore the role of PD-L1 within breast cancer cells and identify key targets for future immunotherapy. Methods: RNA-seq was performed on breast cancer cells with silenced PD-L1 to screen for differentially expressed genes, followed by bioinformatics analysis. Clinical specimens from breast cancer patients undergoing primary surgery without preoperative treatment were collected, along with in vitro analysis to validate the potential mechanism. Results:More >

  • Open Access

    CORRECTION

    CORRECTION: MiR-150-5p Inhibits Cell Proliferation and Metastasis by Targeting FTO in Osteosarcoma

    LICHEN XU1,2, PAN ZHANG3, GUIQI ZHANG2, ZHAOLIANG SHEN4, XIZHUANG BAI1,3,*

    Oncology Research, Vol.33, No.7, pp. 1797-1798, 2025, DOI:10.32604/or.2024.061279 - 26 June 2025

    Abstract This article has no abstract. More >

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