Publications by authors named "Naoki Oike"

Purpose: Ewing sarcoma (EwS) is the second most common bone cancer in children, accounting for 2% of pediatric cancer diagnoses. Patients who present with metastatic disease at the time of diagnosis have a dismal prognosis, compared to the >70% 5-year survival of those with localized disease. Novel therapeutic approaches that can impact metastatic disease are desperately needed, as well as a deeper understanding of the heterogeneity of EwS tumors.

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  • * The patient group consisted of nearly equal numbers of men and women, with a mean age of 62 years, and the UE procedures were performed by various types of surgeons, including plastic, orthopedic, and general surgeons.
  • * Results showed high rates of inappropriate surgical techniques, with many patients requiring re-excisions and subsequent soft-tissue reconstruction, highlighting the need for improved education on sarcoma management for all surgeons.
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  • Ewing sarcoma is the second most common bone cancer in kids, and those diagnosed with metastatic disease have a poor outlook due to the presence of the EWS/Fli1 fusion gene that drives tumor growth.
  • Research shows that the Wnt/β-Catenin signaling pathway in Ewing sarcoma cells is activated differently depending on the tumor environment, especially in relation to hypoxia and EWS/Fli1 activity.
  • The study identifies CDH11 as a crucial factor in how Wnt/β-Catenin signaling varies among tumor cells, suggesting it could be a potential target for treatment to improve outcomes in Ewing sarcoma patients.
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Ewing sarcoma is the second most common bone cancer in children, accounting for 2% of pediatric cancer diagnoses. Patients who present with metastatic disease at the time of diagnosis have a dismal prognosis, compared to the >70% 5-year survival of those with localized disease. Here, we utilized single cell RNA-sequencing to characterize the transcriptional landscape of primary Ewing sarcoma tumors and surrounding tumor microenvironment (TME).

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  • Deep dermatophytosis is a serious fungal infection that typically affects immunocompromised individuals, linked recently to a deficiency in the CARD9 protein.
  • In a reported case, an 80-year-old Japanese man developed this infection after presenting with skin lesions, leading to severe complications despite antifungal treatment, including the amputation of his left leg.
  • Genetic testing confirmed a specific mutation in the CARD9 gene, highlighting the connection between this deficiency and the exacerbated fungal infection.
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  • - T-cell receptor-engineered therapies show promise for treating synovial sarcoma, but their effectiveness is limited by the need for human leukocyte antigen (HLA) matching, which chimeric antigen receptor (CAR) therapies can potentially bypass by targeting tumor-associated antigens directly.
  • - Researchers analyzed synovial sarcoma cell lines and found that ligands for NK cell-activating receptors like NKp44 and NKp30 were expressed, while others like NKp46 had no expression, suggesting potential for targeted therapy.
  • - The study indicated that NKp44-based CAR T cells could specifically recognize and suppress synovial sarcoma cell growth, making CAR therapies a viable option for this type of cancer treatment.
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Introduction: Fine needle aspiration cytology (FNAC) and core needle biopsy (CNB) can provide tissue samples for the diagnoses of bone and soft tissue tumors. We evaluated the diagnostic accuracy of FNAC and CNB, the usefulness of the image-guided needle procedures, and assessed whether a discordance can influence the prognosis.

Patients And Methods: We retrospectively examined the accuracy rates of FNAC and CNB procedures by analyzing results of 405 specimens of 389 patients.

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Background: Synovial sarcoma is a rare malignant soft-tissue tumor that is prevalent in adolescents and young adults, and poor prognosis has been reported in patients with metastatic lesions. Chimeric antigen receptor (CAR) T-cell therapy is an emerging novel therapy for solid tumors; however, its application in synovial sarcoma has not yet been explored.

Methods: A novel human epidermal growth factor receptor 2 (HER2)-targeted CAR containing scFv-FRP5, CD8α hinge and transmembrane domains as well as 4-1BB costimulatory and CD3ζ signaling domains was developed.

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The characteristics of the tumor immune microenvironment remains unclear in liposarcomas, and here we aimed to determine the prognostic impact of the tumor immune microenvironment across separate liposarcomas subtypes. A total of 70 liposarcoma patients with three subtypes: myxoid liposarcoma (n = 45), dedifferentiated liposarcoma (n = 17), and pleomorphic liposarcoma (n = 8) were enrolled. The presence of tumor infiltrating lymphocytes (CD4+ , CD8+ , FOXP3+ lymphocytes) and CD163+ macrophages and expression of HLA class I and PD-L1 were assessed by immunohistochemistry in the diagnostic samples; overall survival and progression-free survival were estimated from outcome data.

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Stanniocalcin-1 () is a glycoprotein that was originally identified as a calcium-regulating hormone in bony fish, and that has been shown to also critically mediate cell growth, proliferation and differentiation, etc. in humans. Increased expression levels have been previously detected in different human cancer samples, such as those isolated from lung, breast, ovary, colon, pancreas, and liver tumors; thus, the present study evaluated expression in various soft-tissue tumors.

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Background: Patellar tendon autograft after intraoperative extracorporeal radiotherapy has been used for reconstruction of the extensor mechanism following limb-sparing wide tumor resection around the knee. The purpose of this study was to determine the clinical outcome of this reconstruction technique.

Methods: We retrospectively reviewed six consecutive patients with peripatellar tendon and proximal tibial sarcoma who underwent reconstruction of the knee extensor mechanism.

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Bone and soft tissue tumors are derived from mesenchymal cells, and they are hard to treat. Receptor-activator of nuclear factor-kappa B ligand (RANKL) is an essential cytokine for osteoclast differentiation and activation and is expressed on the surface of osteoblasts or stromal cells. In this study, to explore the potential of denosumab treatment for soft tissue tumors, we analyzed the expression profiles of RANKL mRNA in 425 tumor specimens of 33 histological types by real-time RT-PCR.

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The natural history of asymptomatic retroperitoneal schwannomas is poorly understood. This study aimed at investigating the natural history of incidental retroperitoneal schwannomas. The medical charts and imaging studies of 22 asymptomatic patients under observation for at least 12 months for retroperitoneal schwannomas were reviewed.

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  • * Researchers analyzed immune cell infiltration and key immune markers in 36 patients, finding that CD8+ and FOXP3+ lymphocyte levels correlated with better survival, while CD163+ macrophages were linked to worse outcomes.
  • * The findings highlight the importance of the tumor immune microenvironment, suggesting that specific immune cell types could serve as potential prognostic indicators for patients with synovial sarcoma.
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Bone leiomyosarcoma is a rare primary osseous malignant tumor with a high metastatic potential. Similar to other bone sarcomas, high histological grade and tumor stage are predictive of a poor outcome. We herein present our experience with treating a 64-year-old woman with bone leiomyosarcoma accompanied by multiple bone metastases.

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Background: A solitary fibrous tumour (SFT) is an unusual neoplasm typically found in soft tissues. Although SFTs can arise in the bones, they very rarely arise in the vertebral arch. Here, we describe a case of a SFT that arose in the vertebral arch of the first lumbar (L1) spinal vertebrae and mimicked osteosarcoma.

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The prognosis of alveolar soft part sarcoma is poor, despite the slow growth of the tumor. A number of cases with spontaneous regression of this rare tumor have been reported. Although the mechanisms underlying spontaneous regression remain uncertain, local immune reaction may be a possible contributing factor.

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Intravertebral cleft (IVC) is a common finding in osteoporotic compression fracture. However, since the vertebral collapse attributable to cancer metastasis is rarely associated with IVC, the phenomenon is generally considered as a sign of a benign lesion. In this study, we retrospectively reviewed the radiographs, computed tomography scans, and magnetic resonance images of 111 patients with spinal metastasis.

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The Niigata Prefectural Central Hospital (NPCH) is one of the main hospitals for the cities of Joetsu and Myoko, Niigata Prefecture, Japan, an area with a population of 240,141, of whom 26.7 % were aged ≥65 years in 2009. In the NPCH, patients with hip fractures are admitted to an orthopedic ward within 4 h, 89.

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Soft tissue tumors arising in deep veins of the extremities are uncommon, although a few cases of synovial sarcoma or leiomyosarcoma arising in the femoral vein have been documented. However, to the best of our knowledge, an extraskeletal myxoid chondrosarcoma (EMC) arising in the femoral vein has not been reported in the English literature. We report a case of EMC arising in the femoral vein of a 70-year-old man who presented with right leg edema and was diagnosed with a deep venous thrombosis (DVT) by computed tomography (CT).

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