https://aseestant.ceon.rs/index.php/aoo/issue/feed Archive of Oncology 2026-04-17T10:23:11+02:00 Archive of Oncology archive@onk.ns.ac.rs SCIndeks Assistant Archive of Oncology covers resources on the mechanism, cause, and treatment of cancer including environmental and genetic risk factors, and cellular and molecular carcinogenesis https://aseestant.ceon.rs/index.php/aoo/article/view/66550 Impressum 2026-04-17T10:23:09+02:00 Archive of Oncology archive@onk.ns.ac.rs 2026-04-16T10:28:11+02:00 Copyright (c) 2026 Archive of Oncology https://aseestant.ceon.rs/index.php/aoo/article/view/66551 Editorial Board 2026-04-17T10:23:09+02:00 Archive of Oncology archive@onk.ns.ac.rs 2026-04-16T10:31:41+02:00 Copyright (c) 2026 Archive of Oncology https://aseestant.ceon.rs/index.php/aoo/article/view/59783 Acceptance of human papilloma virus self-testing in cervical cancer prevention among rural Nigerian women 2026-04-17T10:23:09+02:00 Matilda Kerry matilda.kerry@npmcn.edu.ng Ifeoma Okafor iokafor@unilag.edu.ng Alero Roberts aaroberts@cmul.edu.ng Mobolanle Balogun mbalogun@cmul.edu.ng Omolara Oyadotun laraoyadotun@yahoo.com Awofeso Opeyemi awofesoopeyemi@gmail.com Uzoamaka Igwilo uzoamakaigwilo@gmail.com Tope Olubodun Olubodun oluboduntope@gmail.com Damilola Akinsulire damilola.akinsulire@northlincs.gov.uk Ugonna Igwilo Igwilo ugonnaigwilo@gmail.com <p class="MsoNormal" style="margin-bottom: .0001pt; text-align: justify; text-justify: inter-ideograph; line-height: normal;"><strong><span lang="EN-GB" style="font-size: 12pt; font-family: 'Times New Roman', 'serif'; color: #0d0d0d; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">Background: </span></strong><span lang="EN-GB" style="font-size: 12pt; font-family: 'Times New Roman', 'serif'; color: #0d0d0d; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">This study investigates the knowledge and acceptance of human papillomavirus (HPV) self-testing among rural women in Badagry, Lagos State, Nigeria, aiming to address the growing public health concern of cervical cancer. With 9,922 new cervical cancer cases annually in Nigeria, late diagnosis and suboptimal treatment contribute to high mortality rates. </span></p> <p class="MsoNormal" style="margin-bottom: .0001pt; text-align: justify; text-justify: inter-ideograph; line-height: normal;"><strong><span lang="EN-GB" style="font-size: 12pt; font-family: 'Times New Roman', 'serif'; color: #0d0d0d; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">Methods: </span></strong><span lang="EN-GB" style="font-size: 12pt; font-family: 'Times New Roman', 'serif'; color: #0d0d0d; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">The study involved 220 women who performed HPV self-sampling alongside physician-conducted visual inspection with acetic acid (VIA) and reported preference. </span></p> <p class="MsoNoSpacing" style="text-align: justify; text-justify: inter-ideograph;"><strong><span lang="EN-US" style="font-size: 12pt; font-family: 'Times New Roman', 'serif'; color: #0d0d0d; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">Results: </span></strong><span lang="EN-US" style="font-size: 12pt; font-family: 'Times New Roman', 'serif'; color: #0d0d0d; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">The results reveal inadequate cervical cancer awareness (55.5%) and low HPV knowledge (20.9%), particularly among women with incomplete education. While 80.9% of women preferred VIA, only 49.1% found HPV self-sampling feasible. Notably, self-testing was more accepted among divorced, separated, and widowed women.</span></p> <p class="MsoNormal" style="margin-bottom: .0001pt; text-align: justify; text-justify: inter-ideograph; line-height: normal;"><strong><span lang="EN-GB" style="font-size: 12pt; font-family: 'Times New Roman', 'serif'; color: #0d0d0d; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">Conclusion: </span></strong><span lang="EN-GB" style="font-size: 12pt; font-family: 'Times New Roman', 'serif'; color: #0d0d0d; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">The efforts to improve education and awareness about the causative role of HPV in cervical cancer awareness are crucial to enhance its utilization and acceptance in rural settings.</span></p> <p class="MsoNormal" style="margin-bottom: .0001pt; text-align: justify; text-justify: inter-ideograph; line-height: normal;"><span lang="EN-GB" style="font-size: 12pt; font-family: 'Times New Roman', 'serif'; color: #0d0d0d; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">&nbsp;</span></p> <p>&nbsp;</p> <p class="MsoNormal" style="margin-bottom: .0001pt; text-align: justify; text-justify: inter-ideograph; line-height: normal;">&nbsp;</p> 2026-04-16T10:33:19+02:00 Copyright (c) 2026 Archive of Oncology https://aseestant.ceon.rs/index.php/aoo/article/view/59688 Anticancer activity of eugenol from clove (Syzygium aromaticum L.) against MCF-7 breast cancer cells: in silico and in vitro evaluation 2026-04-17T10:23:10+02:00 Siti Hajar Permatahati Shofyani iti.hajar.permatahati.shofyani@mail.ugm.ac.id Muhammed Evy Prastiyanto wahyuaristyaningputri@ugm.ac.id Daniel Geleta wahyuaristyaningputri@ugm.ac.id Wahyu Putri wahyuaristyaningputri@ugm.ac.id <p class="MsoNormal" style="text-align: justify; line-height: 200%;"><span lang="EN-ID" style="font-size: 12.0pt; line-height: 200%; font-family: 'Times New Roman','serif';">Breast cancer is a major cause of cancer-related deaths among women globally. Despite notable progress in the treatment options, the pursuit of effective natural-based therapeutic alternatives continues to be essential. <em>Syzygium aromaticum L</em>. (cloves) is rich in eugenol, a phenolic compound known for its antimicrobial, anti-inflammatory, and anticancer effects. This study aimed to assess the anticancer activity of eugenol extracted from cloves against MCF-7 breast cancer cells using in silico molecular docking and <em style="mso-bidi-font-style: normal;">in vitro</em> cytotoxicity assays. The cloves collected from Natuna District and Magetan District (Indonesia) were extracted through Soxhlet extraction with n-hexane and maceration with ethanol. Gas Chromatography-Mass Spectrometry (GC-MS) analysis identified eugenol as the primary component, making up 53.6% of the Soxhlet extract. The molecular docking results indicated that eugenol has significant binding affinities for AKT (-5.1 kcal/mol) and ESR1 (-5.9 kcal/mol), two essential proteins involved in the proliferation and survival of breast cancer cells. Cytotoxicity assessments using the MTT assay revealed a dose-dependent decrease in MCF-7 cell viability, with notable inhibition occurring at concentrations between 15.625 and 2.000 ppm. These results suggest that the eugenol-rich clove extract demonstrates promising anticancer potential by exerting direct cytotoxic effects and influencing key molecular targets within the breast cancer signalling pathway. </span></p> 2026-04-16T10:39:16+02:00 Copyright (c) 2026 Archive of Oncology https://aseestant.ceon.rs/index.php/aoo/article/view/61577 Multidisciplinary surgical approach in the treatment of giant mucinous ovarian cystadenocarcinoma 2026-04-17T10:23:10+02:00 Jelena Ćurčić curcic.jelena98@gmail.com Borislav Golijan borislav.golijan@gmail.com Jelena Nikolić jelena.nikolic@mf.uns.ac.rs Dragan Stajić dragan.stajic@mf.uns.ac.rs Aleksandar Ćurčić aleksandar.curcic@mf.uns.ac.rs <p class="MsoNormal" style="margin: 0cm; line-height: 29.3333px; font-size: 11pt; font-family: Calibri, sans-serif; text-align: justify;"><strong><span lang="EN-US" style="font-size: 12pt; line-height: 32px; font-family: 'Times New Roman', serif;">Introduction</span></strong><span lang="EN-US" style="font-size: 12pt; line-height: 32px; font-family: 'Times New Roman', serif;">: Giant ovarian tumors (&gt;20 cm) are not common and often present late, with organ compression symptoms and increased abdominal girth. Early diagnosis is challenging due to nonspecific complaints until tumors reach massive dimensions.</span></p> <p class="MsoNormal" style="margin: 0cm; line-height: 29.3333px; font-size: 11pt; font-family: Calibri, sans-serif; text-align: justify;"><strong><span lang="EN-US" style="font-size: 12pt; line-height: 32px; font-family: 'Times New Roman', serif;">Case Presentation:</span></strong><span lang="EN-US" style="font-size: 12pt; line-height: 32px; font-family: 'Times New Roman', serif;"> A 49‑year‑old woman presented with progressive abdominal distension over, as she claimed, four months, culminating in a 180-cm abdominal circumference that impaired mobility and caused orthopnea. Contrast‑enhanced CT demonstrated a 54 &times; 26 &times; 25 cm cystic mass of ovarian origin, with focal wall thickening up to 5.6 cm, displacing abdominopelvic organs and elevating diaphragm. After multidisciplinary consultation, a midline laparotomy was performed. Controlled puncture and aspiration yielded approximately 53 L of mucinous fluid. A right adnexectomy was performed, and frozen‑section analysis indicated a borderline mucinous tumor. The operation continued with total hysterectomy, left adnexectomy, and partial omentectomy. Abdominal closure was achieved by abdominal and plastic surgeons: excess fascia and skin were excised, a synthetic mesh was placed, and abdominoplasty was performed. Definitive histopathology and immunohistochemistry confirmed right ovary mucinous cystadenocarcinoma without capsular surface involvement or lymphovascular invasion, staged as FIGO IC1. The patient received six cycles of adjuvant paclitaxel&ndash;carboplatin. At one‑year follow‑up, the patient exhibited no evidence of recurrence and satisfactory abdominal contour.</span></p> <p class="MsoNormal" style="margin: 0cm; line-height: 29.3333px; font-size: 11pt; font-family: Calibri, sans-serif; text-align: justify;"><strong><span lang="EN-US" style="font-size: 12pt; line-height: 32px; font-family: 'Times New Roman', serif;">Conclusion</span></strong><span lang="EN-US" style="font-size: 12pt; line-height: 32px; font-family: 'Times New Roman', serif;">: Management of giant ovarian tumors demands meticulous preoperative planning and a coordinated multidisciplinary team. Surgical challenges include safe tumor decompression, accurate intraoperative diagnosis, and specialized abdominal wall reconstruction including gynecologic, abdominal, and plastic surgical expertise.</span></p> <p><strong><span style="font-size: 12.0pt; line-height: 107%; font-family: 'Times New Roman','serif'; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: EN-US; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;">Keywords</span></strong><span style="font-size: 12.0pt; line-height: 107%; font-family: 'Times New Roman','serif'; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: EN-US; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;">: giant ovarian tumors, borderline ovarian tumor, mucinous cystadenocarcinoma.</span></p> 2026-04-16T00:00:00+02:00 Copyright (c) 2026 Archive of Oncology https://aseestant.ceon.rs/index.php/aoo/article/view/59950 Gigantic hip mass as the initial presentation of hyperphosphatemic familial tumoral calcinosis 2026-04-17T10:23:10+02:00 Surya Krishnan suryaradhakrishnan28@gmail.com Anjali Murali anjalivakkom@gmail.com Pavithran Keechilat drkpavithran@gmail.com <p style="margin: 0cm; margin-bottom: .0001pt; text-align: justify;"><strong><span lang="EN-IN">Introduction:</span></strong><span lang="EN-IN"> Hyperphosphatemic familial tumoural calcinosis (HFTC) is a rare autosomal recessive disorder characterised by ectopic calcium phosphate deposition around the joints due to mutations affecting phosphate regulation.</span></p> <p style="margin: 0cm; margin-bottom: .0001pt; text-align: justify;"><strong><span lang="EN-IN">Case outline:</span></strong><span lang="EN-IN"> We report a 7-year-old boy who presented with hip pain and swelling, mimicking malignancy. Imaging revealed a large lobulated soft tissue mass involving the left iliac fossa and pelvic musculature. The FDG-PET and MRI findings suggested a neoplastic lesion, but the FNAC revealed only calcific debris. Biochemical analysis revealed elevated serum phosphorus levels and low PTH. Whole-exome sequencing identified a homozygous likely pathogenic mutation in <em style="mso-bidi-font-style: normal;">GALNT3</em> (c.840T&gt;A; p.Cys280Ter). Medical management included phosphate binders and acetazolamide. Despite initial improvement, recurrence occurred one year later. Surgical options were deemed high-risk and conservative treatment was continued.</span></p> <p style="margin: 0cm; margin-bottom: .0001pt; text-align: justify;"><strong><span lang="EN-IN">Conclusion:</span></strong><span lang="EN-IN"> This case highlights the importance of considering HFTC in the differential diagnosis of calcified soft tissue masses in children and the role of genetic testing in diagnosis and management.</span></p> 2026-04-16T10:47:02+02:00 Copyright (c) 2026 Archive of Oncology https://aseestant.ceon.rs/index.php/aoo/article/view/58166 Management of giant desmoid type fibromatosis of abdominal wall 2026-04-17T10:23:10+02:00 Jelena Nikolić jelena.nikolic@mf.uns.ac.rs Marija Marinković marija.marinkovic@mf.uns.ac.rs Mladen Jovanović mladen.jovanovic@mf.uns.ac.rs Teodora Tubić teodora.tubic@mf.uns.ac.rs Vanja Tatalović vanja.tatalovic@mf.uns.ac.rs <p class="MsoNormal" style="margin: 0in; font-size: medium; font-family: Aptos, sans-serif; text-align: justify; line-height: 24px;"><strong><span lang="EN-GB" style="font-family: 'Times New Roman', serif;">Introduction.</span></strong><span lang="EN-GB" style="font-family: 'Times New Roman', serif;">&nbsp;Desmoid type fibromatosis (DT) represents a rare benign tumor formations characterized with local aggressive behaviour, but absence of metastatic potential. Histologically they are often misdiagnosed leading to unnecessary radical surgery. Even with proper diagnose there are different approaches and not clear protocols for treatment of DT.&nbsp;</span></p> <p class="MsoNormal" style="margin: 0in; font-size: medium; font-family: Aptos, sans-serif; text-align: justify; line-height: 24px;"><strong><span lang="EN-GB" style="font-family: 'Times New Roman', serif;">Case report</span></strong><span lang="EN-GB" style="font-family: 'Times New Roman', serif;">. The study presents the case of 33-year-old male that presented in emergency department with large swelling of abdominal wall that was present for two years. Ultrasound was done and abdominal swelling was described by radiologist as ventral hernia. After further radiological studies (CT scan and magnetic resonance) diagnosis of tumour of abdominal wall was established. Biopsy led to diagnose of sarcoma. Surgery was planned as tumour was growing rapidly reaching around 30 cm and producing necrosis of abdominal wall skin. After resection of 8.5kg of tumour and clinically clear margins defect was reconstructed by placing polypropylene mesh and darn Nylon suture with local rotational skin flap. In the postoperative days an infection of surgical wound developed. Infection was resolved in two weeks without further complications. The definitive histopathological diagnoses was desmoid type fibromatosis.&nbsp;</span></p> <p class="MsoNormal" style="margin: 0in; font-size: medium; font-family: Aptos, sans-serif; text-align: justify; line-height: 24px;"><strong><span lang="EN-GB" style="font-family: 'Times New Roman', serif;">Conclusion</span></strong><span lang="EN-GB" style="font-family: 'Times New Roman', serif;">. Active surveillance is considered today as most acceptable strategy in treatment of DT. Better understanding of genetic alterations which are in base of DT and determining prognostic factors that favour aggressive behaviour, will lead to creation of appropriate individual strategy and tailored therapy for every patient.</span></p> 2026-04-16T10:48:08+02:00 Copyright (c) 2026 Archive of Oncology https://aseestant.ceon.rs/index.php/aoo/article/view/63428 Erratum to: Comparation of animal models of acute toxicity of doxorubicin (Vol 31(2);3-8, 2025) 2026-04-17T10:23:10+02:00 Archive of Oncology archive@onk.ns.ac.rs <p class="mdpi17abstract" style="margin: 0cm; margin-bottom: .0001pt; text-align: justify;"><strong><span lang="EN-US">Background</span></strong><span lang="EN-US">: Animal models are essential for research in biomedicine. The cardiotoxicity of doxorubicin is the most common and severe side effect of this potent chemotherapeutic agent, and in order to investigate its prevention, a large number of studies have been performed on animal models. Unfortunately, the models are not uniform and the applied doses as well as the effectiveness vary significantly, often with great animal suffering.</span></p> <p class="mdpi17abstract" style="margin: 0cm; margin-bottom: .0001pt; text-align: justify;"><strong><span lang="EN-US">Methods</span></strong><span lang="EN-US">: Male Wistar rats were divided into three groups of 10 animals each and treated with saline solution intraperitoneally (group C), or with doxorubicin intraperitoneally in a single dose of 15 mg/kg (group G15) or 20 mg/kg (group G20). Body weight, mortality, the condition of animals, intensity of lipid peroxidation, activity of antioxidant enzymes and myocardial tissue damage (using doxorubicin damage score, DDS) were analyzed.</span></p> <p class="mdpi17abstract" style="margin: 0cm; margin-bottom: .0001pt; text-align: justify;"><strong><span lang="EN-US">Results</span></strong><span lang="EN-US">: Group 20, in comparison with groups G15 and C, exhibited the worse general condition, higher mortality and significantly higher intensity of lipid peroxidation. Both doses of doxorubicin induced a statistically significant decrease of&nbsp;<span style="letter-spacing: -0.1pt;">superoxide dismutase (SOD),&nbsp;</span>glutathione peroxidase (GSH-Px), and glutathione-S-transferase (GST)&nbsp;activity compared to the control group<span style="letter-spacing: -0.15pt; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">.</span>&nbsp;Among the doxorubicin-treated groups, GR is significantly more reduced in G15. GST is significantly more reduced in G20 while SOD and GSH-Px do not differ. The DDS score indicates myocardial tissue injury in both G15 and G20.</span></p> <p>&nbsp;</p> <p class="mdpi17abstract" style="margin: 0cm; margin-bottom: .0001pt; text-align: justify;"><strong><span lang="EN-US">Conclusions</span></strong><span lang="EN-US">: Both applied doses induce animal models of acute doxorubicin induced oxidative stress and cardiotoxicity. A higher dose is more suitable for studies of oxidative stress, but should be applied with caution due to higher mortality. A lower dose is more suitable for studies focused on tissue morphology.</span></p> 2026-04-16T10:49:08+02:00 Copyright (c) 2026 Archive of Oncology https://aseestant.ceon.rs/index.php/aoo/article/view/66552 Instructions for Authors 2026-04-17T10:23:11+02:00 Archive of Oncology archive@onk.ns.ac.rs 2026-04-16T10:54:45+02:00 Copyright (c) 2026 Archive of Oncology