OncosciencePub Date : 2026-04-28eCollection Date: 2026-01-01DOI: 10.18632/oncoscience.657
Maya Kulshekar, Anuradha B Patil, Rajendra B Nerli
{"title":"Modifiable risk factors of prostate cancer: Insights from a hospital-based study.","authors":"Maya Kulshekar, Anuradha B Patil, Rajendra B Nerli","doi":"10.18632/oncoscience.657","DOIUrl":"10.18632/oncoscience.657","url":null,"abstract":"<p><strong>Introduction: </strong>Prostate Cancer (PCa) is the second most common cancer and the fifth leading cause of cancer among men worldwide. The prevalence of Prostate cancer is much lower in India and it is likely that the incidence of prostate cancer will show an increase in the future. Modifiable habits like smoking, tobacco chewing, alcohol consumption and others have shown to be associated with Prostate Cancer. All these variables show conflicting results in various studies. Hence more research on the various determinants of Prostate Cancer for the Indian population will help in reducing the burden of this disease through scientific and empirical approach. The present study aims to study association of various modifiable risk factors with Prostate Cancer and Benign Prostatic Hyperplasia.</p><p><strong>Methods: </strong>72 histologically proven prostate 'Cancer Cases' and 132 'BPH controls' were included for the study after obtaining their Informed Consent. This was confirmed by performing the PSA (Prostate Specific Antigen Test), DRE (Digital Rectal Examination) test and histopathological investigations. Odds ratio was obtained to study the association of the risk factors.</p><p><strong>Results: </strong>Our study revealed that Modifiable risk factors associated with decreased risk of Prostate cancer are Coffee intake and meat with an odds ratio of 0.355 (95% CI 0.175 to 0.72, <i>p</i> = 0.004) and 0.516 (95% CI 0.269 to 0.992, <i>p</i> = 0.047). No significant association was observed with other modifiable risk factors.</p><p><strong>Conclusions: </strong>The present study concludes that an increased intake of coffee and meat may be linked to a reduced risk of developing prostate cancer.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"143-151"},"PeriodicalIF":0.0,"publicationDate":"2026-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13141943/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147848094","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OncosciencePub Date : 2026-04-15eCollection Date: 2026-01-01DOI: 10.18632/oncoscience.656
Reshmi Sultana, A M Adarsha, Tushar M Parmeshwar, Akula Nynasindhu, Abhimanyu Sharma
{"title":"Ileal leiomyoma disguised as intussusception: Imaging pitfalls in a 28-year-old female.","authors":"Reshmi Sultana, A M Adarsha, Tushar M Parmeshwar, Akula Nynasindhu, Abhimanyu Sharma","doi":"10.18632/oncoscience.656","DOIUrl":"10.18632/oncoscience.656","url":null,"abstract":"<p><p>Leiomyomas are benign mesenchymal tumors that commonly occur in uterus and rarely in gastrointestinal tract with esophagus being the most frequent site followed by stomach and colon. Duodenal leiomyoma is rarest of all with ileal leiomyoma being the second rarest. This report discusses a case of a 28-year-old female with an enlarging lower abdominal mass post-hysterectomy, initially misinterpreted as an adnexal tumor based on imaging. Various diagnostic modalities, including ultrasound, CECT, and MRI, provided conflicting interpretations, complicating preoperative assessment. Exploratory laparotomy confirmed an intraluminal ileal leiomyoma, highlighting the importance of integrated imaging and histopathological evaluation for accurate diagnosis. Genetic studies indicate associations with syndromic conditions like NF1 and Reed syndrome, emphasizing the need for vigilant surveillance and potential molecular-targeted therapies. While traditionally managed surgically, emerging research suggests epigenetic modifications may play a role in tumor behaviour and therapeutic advancements.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"138-142"},"PeriodicalIF":0.0,"publicationDate":"2026-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13142175/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147848128","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OncosciencePub Date : 2026-04-02eCollection Date: 2026-01-01DOI: 10.18632/oncoscience.655
Gunvanti Rathod, Monica Mishra, Banka Sai Swetha, Siddharam S Janti, Shamli D Zalke, Kolavali Raghavendra Rao, Alisha Khan
{"title":"Sebaceous adenoma of the eyelid: A clinical, histopathological, and immunohistochemical perspective.","authors":"Gunvanti Rathod, Monica Mishra, Banka Sai Swetha, Siddharam S Janti, Shamli D Zalke, Kolavali Raghavendra Rao, Alisha Khan","doi":"10.18632/oncoscience.655","DOIUrl":"10.18632/oncoscience.655","url":null,"abstract":"<p><p>Sebaceous adenoma (SA) is a rare, slow-growing benign tumor arising from sebaceous glands, accounting for less than 0.5% of all cutaneous neoplasms and approximately 1-2% of eyelid tumors. The eyelid is an uncommon site for this lesion. Histologically, SA shows well-circumscribed lobules composed of mature sebocytes with vacuolated cytoplasm and a peripheral rim of basaloid cells, without nuclear atypia or mitotic activity. We report a case of an 81-year-old man with a unilateral papillomatous lesion in the left lower eyelid, diagnosed as sebaceous adenoma on histopathology. Immunohistochemistry revealed EMA positivity and a low Ki-67 proliferative index, confirming its benign nature. The rarity of its pseudopapillomatous presentation and its need for differentiation from sebaceous carcinoma highlight the diagnostic importance of this case.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"130-137"},"PeriodicalIF":0.0,"publicationDate":"2026-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13142177/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147848117","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OncosciencePub Date : 2026-04-02eCollection Date: 2026-01-01DOI: 10.18632/oncoscience.654
Joseph A Bauer, Annette M Sysel, Michael J Dunphy
{"title":"Selective blood-brain barrier penetration and tumor targeting of nitrosylcobalamin in glioblastoma: Pharmacokinetics, tissue distribution, and synergistic activity with trail and temozolomide.","authors":"Joseph A Bauer, Annette M Sysel, Michael J Dunphy","doi":"10.18632/oncoscience.654","DOIUrl":"10.18632/oncoscience.654","url":null,"abstract":"<p><strong>Background: </strong>Glioblastoma multiforme (GBM) remains a lethal brain tumor characterized by poor response to chemotherapy and limited blood-brain barrier (BBB) permeability. Nitrosylcobalamin (NO-Cbl), a nitric oxide (NO)-releasing cobalamin analog, was developed to selectively deliver cytotoxic NO to tumors through the transcobalamin II receptor (CD320).</p><p><strong>Methods: </strong>NO-Cbl was evaluated across the NCI-60 tumor panel, followed by pharmacokinetic and biodistribution studies in glioblastoma-bearing rats using nitrate and cobalamin quantification in tissues, serum, and cerebrospinal fluid (CSF). Synergistic activity with TRAIL or temozolomide was assessed in human U87 and D54 glioma cells using SRB assays and Chou-Talalay analysis.</p><p><strong>Results: </strong>NO-Cbl showed broad antitumor activity <i>in vitro</i>, with central nervous system tumor cell lines displaying intermediate sensitivity (mean ID50 = 17.6 μM). <i>In vivo</i>, NO-Cbl effectively crossed the BBB, with tumor nitrate levels peaking at 20.4 nmol/g at 30 min and remaining elevated at 24 h, confirming tumor-selective accumulation. Serum nitrate exhibited a rapid half-life (4-5 h), while serum and CSF B12 showed slower and variable clearance (21-26 h and 11-12 h, respectively). In glioma cell lines, NO-Cbl synergized with TRAIL and temozolomide (TMZ) (combination index < 1.0), enhancing antiproliferative effects and suggesting potential to overcome resistance mechanisms.</p><p><strong>Conclusion: </strong>This pilot study demonstrates that NO-Cbl crosses the BBB, accumulates selectively in brain tumor tissue, and synergizes with established and experimental glioblastoma therapies. These findings establish a translational foundation for developing cobalamin-based therapeutics as a novel treatment strategy for glioblastoma.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"120-129"},"PeriodicalIF":0.0,"publicationDate":"2026-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13142176/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147848133","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OncosciencePub Date : 2026-03-19eCollection Date: 2026-01-01DOI: 10.18632/oncoscience.653
Benjamin Wenyuan Xie, Shreyas Kalantri
{"title":"Unprecedented non-luminal esophageal adenocarcinoma invading the spine.","authors":"Benjamin Wenyuan Xie, Shreyas Kalantri","doi":"10.18632/oncoscience.653","DOIUrl":"10.18632/oncoscience.653","url":null,"abstract":"<p><strong>Background: </strong>Upper endoscopy with biopsy is the gold standard for diagnosing esophageal cancer. However, esophageal tumors can rarely escape endoscopic detection by growing in atypical patterns, such as entirely outside the esophageal lumen.</p><p><strong>Case: </strong>We report a unique case of primary esophageal adenocarcinoma that presented with spinal cord compression due to local invasion of the T5 vertebral body, despite an initially normal upper endoscopy. A 68-year-old man developed progressive paraparesis and sensory loss due to a T5 pathological fracture. He had classic symptoms of esophageal cancer (dysphagia and weight loss), yet endoscopic evaluation one month prior showed no intraluminal tumor. Imaging revealed a posterior mediastinal mass contiguous with the esophagus and invading the T4-T6 vertebrae. Surgical resection of the epidural tumor confirmed poorly differentiated adenocarcinoma consistent with an esophageal primary. The patient declined chemoradiation and succumbed one month later.</p><p><strong>Conclusions: </strong>This unprecedented pattern of esophageal adenocarcinoma-growing extraluminally with isolated posterior extension to the spine-highlights the potential for esophageal cancer to present with no mucosal lesion on endoscopy. Clinicians should remain vigilant for malignancy in patients with high suspicion, even if initial endoscopic findings are benign.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"115-119"},"PeriodicalIF":0.0,"publicationDate":"2026-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13248710/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148221315","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OncosciencePub Date : 2026-03-11eCollection Date: 2026-01-01DOI: 10.18632/oncoscience.652
Faisal Iqbal
{"title":"A low-cost color sensor device for rapid detection of high-grade serous ovarian carcinoma (HGSOC).","authors":"Faisal Iqbal","doi":"10.18632/oncoscience.652","DOIUrl":"10.18632/oncoscience.652","url":null,"abstract":"<p><p>A sensitive nucleic acid detection approach based on tracing the inorganic phosphate (Pi) created during amplification by means of the colorimetric method has been presented. This method relies on nucleic acid amplification. Pyrophosphate (PPi), a result of the nucleic acid polymerization reaction, was hydrolyzed into inorganic phosphate (Pi) by the addition of inorganic pyrophosphatase. To create the phosphomolybdate precipitate, the obtained Pi could react with acid molybdate. The color of amplified sample was changed into green. Using high grade serous ovarian carcinoma (HGSOC) as an example, this tactic's usefulness was proven. Here, describe the Ercose (Eraser + Color Sensor) device proof-of-concept, which uses a straightforward strategy without sacrificing the accuracy of the outcomes. Ercose is a simple, quick, weightless and inexpensive. A low-cost, user-friendly color sensor is suggested for development in this study to identify the hue of the objects. The test objects were progressively illuminated by the sensor's RGB light emitting diodes, which served as the light sources. The analogue voltage data were converted to digital form and serially delivered to a graphical user interface (GUI). To determine the test objects colors, the digitized voltage values were employed (i.e., RGB values). The microcontroller arduino nano was managed by the GUI, which also showed the needed color values. The Ercose device can be used in a variety of real-world scenarios where standard spectrophotometer devices are not practical.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"104-114"},"PeriodicalIF":0.0,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12998687/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147488834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Deceptive clinical course of mucinous ovarian carcinoma mimicking pelvic abscess in a postmenopausal woman: An exceptional case report.","authors":"Aparna Jarathi, Sunitha Geddada, Chandramouli Ramalingam, Naina Kumar, Anusha Devalla, Ashwini Pitambra, Ashutosh Rath, NagaSai Divya Kari, Uday Reddy Janke, B Surender Reddy, Ajay Kumar Kondeti","doi":"10.18632/oncoscience.650","DOIUrl":"10.18632/oncoscience.650","url":null,"abstract":"<p><strong>Background: </strong>Mucinous ovarian carcinoma (MOC) is a rare subtype of epithelial ovarian cancer (3-5%), typically affecting women between 20 and 40 years old. It often presents diagnostic and management challenges.</p><p><strong>Case report: </strong>We present an exceptional case of a postmenopausal woman with abdominal pain disguised as a pelvic abscess. A 73-year-old postmenopausal woman presented with abdominal pain for 6 months and postmenopausal spotting for 1 month. Initial imaging (CT scan) suggested a pelvic abscess, which was managed conservatively. However, persistent symptoms and a complex adnexal mass prompted further evaluation. MRI revealed a multiloculated right adnexal mass, and tumour markers (CA-125, CEA, HE4) were elevated. Surgical staging included total abdominal hysterectomy, bilateral salpingo-oophorectomy, and omentectomy. Histopathology confirmed stage IC2 mucinous adenocarcinoma. Postoperative recovery was uneventful, and the patient received six cycles of carboplatin and paclitaxel as adjuvant chemotherapy.</p><p><strong>Conclusions: </strong>This case emphasizes the diagnostic challenge of MOC in postmenopausal women. Misinterpretation as benign pelvic pathology can delay appropriate treatment. Precise imaging, tumour markers, and a multidisciplinary approach are critical for early diagnosis and improved outcomes.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"80-84"},"PeriodicalIF":0.0,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12998691/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147488926","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Erosive pustular dermatosis-like scalp reaction following cranial radiotherapy in a patient with EGFR-mutant NSCLC treated with amivantamab.","authors":"Vasiliki Nikolaou, Antonis Tsimpidakis, Ioannis-Alexios Koumprentziotis, Evdoxia Panou, Theodoros Tegos, Alexander Stratigos","doi":"10.18632/oncoscience.649","DOIUrl":"10.18632/oncoscience.649","url":null,"abstract":"<p><p>Amivantamab, a bispecific monoclonal antibody directed against the epidermal growth factor receptor (EGFR) and mesenchymal-epithelial transition factor (MET), has demonstrated significant clinical activity and is increasingly incorporated into frontline regimens for EGFR-mutant non-small cell lung cancer (NSCLC). Its increasing clinical use has, nevertheless, been paralleled by recognition of distinctive cutaneous adverse events, most commonly acneiform eruptions, paronychia, and xerosis among others. We present the first case of an erosive pustular dermatosis (EPD)-like reaction limited to a previously irradiated field in a patient receiving amivantamab for EGFR-mutant NSCLC. This case draws attention to the importance of recognizing EPD-like scalp ulcerations as a potential adverse event in patients receiving amivantamab, events that have not been recognized in clinical trials, particularly in the setting of recent or concurrent radiotherapy.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"77-79"},"PeriodicalIF":0.0,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12998686/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147489024","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OncosciencePub Date : 2026-03-11eCollection Date: 2026-01-01DOI: 10.18632/oncoscience.646
Lawik Revend, Doha Revend, Florian Dudde
{"title":"Basal cell carcinoma of the head and neck: Surgical management and postoperative strategies - A researcher's perspective.","authors":"Lawik Revend, Doha Revend, Florian Dudde","doi":"10.18632/oncoscience.646","DOIUrl":"10.18632/oncoscience.646","url":null,"abstract":"<p><strong>Introduction: </strong>Basal cell carcinoma (BCC) is one of the most common cutaneous malignancies and predominantly affects sun-exposed regions, particularly the head and neck. Although metastatic spread is rare, locally invasive growth may compromise functionally and aesthetically critical structures. Effective management therefore requires not only oncologic tumor control but also carefully planned reconstruction and long-term follow-up.</p><p><strong>Materials and methods: </strong>This study presents a structured narrative review of the literature combined with institutional clinical experience. Relevant publications on diagnosis, surgical management, reconstructive techniques, and postoperative strategies for head and neck BCC were identified through searches of PubMed, Embase, and the Cochrane Library. Clinical studies, systematic reviews, and guidelines published between 2000 and 2025 were analyzed and synthesized narratively due to heterogeneity in study designs and outcome measures.</p><p><strong>Results: </strong>Surgical excision remains the cornerstone of curative treatment, with recommended margins depending on tumor risk stratification. Mohs micrographic surgery provides superior margin control in anatomically critical regions. Reconstruction must be individualized based on defect size, anatomical subunit involvement, and patient factors. Local flaps are commonly used for small- to medium-sized defects, whereas larger or deeply infiltrative tumors may require regional or free tissue transfer.</p><p><strong>Discussion: </strong>Successful management of head and neck BCC requires interdisciplinary collaboration and individualized reconstructive planning. Advances in flap techniques, digital surgical planning, and systemic therapies have expanded treatment possibilities, enabling improved functional and aesthetic outcomes in complex cases.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"55-61"},"PeriodicalIF":0.0,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12998690/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147488838","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OncosciencePub Date : 2026-03-11eCollection Date: 2026-01-01DOI: 10.18632/oncoscience.647
Melina A Dattilo, Marina G Ferrari, Alexis P Jimenez-Uribe, Teresa Morales, Kyle T Amber, Adrian P Mansini
{"title":"Targeting MD2 in prostate cancer bone metastasis: Mechanistic insights and therapeutic potential.","authors":"Melina A Dattilo, Marina G Ferrari, Alexis P Jimenez-Uribe, Teresa Morales, Kyle T Amber, Adrian P Mansini","doi":"10.18632/oncoscience.647","DOIUrl":"10.18632/oncoscience.647","url":null,"abstract":"<p><p>Metastatic prostate cancer (PCa), especially when it involves the bone, remains a significant clinical challenge with limited therapeutic options. Our recent research identified Myeloid Differentiation Protein-2 (MD2/LY96) as a potential biomarker associated with poor prognosis and higher metastatic potential in PCa. In this Research Perspective, we build on those findings and present new preclinical data showing that pharmacological inhibition of MD2 markedly reduces tumor growth in a PCa mouse model of bone metastasis. Analysis of patient tumor tissues demonstrated that high MD2 expression is associated not only with metastasis but also with increased infiltration of T regulatory cells (Tregs) and myeloid-derived suppressor cells (MDSCs), indicating a role in promoting an immunosuppressive environment. Additionally, we show that soluble MD2 (sMD2) may serve as a non-invasive biomarker of metastatic burden and help predict resistance to poly ADP-ribose polymerase (PARP) inhibitor therapy. This Research Perspective aims to consolidate mechanistic and preclinical evidence supporting MD2 as a driver of prostate cancer metastasis and to evaluate the therapeutic potential of pharmacological MD2 inhibition in a bone metastasis model. These findings support MD2 as a novel therapeutic target and identify soluble MD2 as a promising predictive and prognostic biomarker in metastatic PCa, with mechanistic links to immune evasion and inflammatory signaling.</p>","PeriodicalId":94164,"journal":{"name":"Oncoscience","volume":"13 ","pages":"62-68"},"PeriodicalIF":0.0,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12998693/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147488997","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}