Faruk Skenderi

Dr. Faruk Skenderi

University of Sarajevo Clinical Center
+1
orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 August 2020 in Cancer Cell International
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Journal Article
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HAHamda Al-Thawadi
Hamda Al-Thawadi
IGIshita Gupta
Ishita Gupta
AJAyesha Jabeen
Ayesha Jabeen
Faruk SkenderiFaruk Skenderi
Faruk Skenderi
TATahar Aboulkassim
Tahar Aboulkassim
Ala-Eddin Al MoustafaAla-Eddin Al Moustafa
Ala-Eddin Al Moustafa
Background: Human papillomaviruses (HPVs) and Epstein–Barr virus (EBV), known oncoviruses, can be co-present and cooperate in the initiation and/or progression of human carcinomas, including head and neck. Based on this fact, we recently reported the prevalence of both HPVs and EBV in cervical and breast cancers.Methods: We herein explore for the first time the co-prevalence of high-risk HPVs and EBV in 98 head and neck (HN) squamous cell carcinoma (SCC) tissues from Bosnian patients using polymerase chain reaction (PCR) and immunohistochemistry (IHC) analysis, as well as tissue microarray methodology.Results: The majority of these cancer tissue cases were from the oral cavity (68%). We found that high-risk HPVs and EBV are co-present in 34.7% of the SCC samples; with a significant correlation between the various HPV types and EBV co-incidence (p = 0.03). Our data showed that 30.8% of oral SCCs are positive for E6 oncoprotein of high-risk HPVs and 44.6% are positive for LMP1 of EBV. The most commonly expressed HPVs in our HNSCC samples include HPV types 16, 18, 45 and 58. Additionally, 37.5% of oral SCCs are positive for both HPVs and EBV, with statistically significant association between high-risk HPV types and EBV (p < 0.05). More importantly, our data revealed that the co-presence of HPV and EBV is strongly correlated with advanced tumor stage (p = 0.035).Conclusion: In this study we show that HPV and EBV oncoviruses are co-present in HNSCC, particularly in oral cancer, where they can cooperate in the initiation and/or progression of this cancer. Thus, further studies are necessary to elucidate the mechanism of this cooperation.

1 April 2017 in Annals of Diagnostic Pathology
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Journal Article
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Faruk SkenderiFaruk Skenderi
Faruk Skenderi
MUMonika Ulamec
Monika Ulamec
TVTomas Vanecek
Tomas Vanecek
PMPetr Martinek
Petr Martinek
RAReza Alaghehbandan
Reza Alaghehbandan
Ondrej HesOndrej Hes
Ondrej Hes

1 August 2020 in Clinical Breast Cancer
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Journal Article
Open access
Semir VranicSemir Vranic
Semir Vranic
PSPhillip Stafford
Phillip Stafford
JPJuan Palazzo
Juan Palazzo
Faruk SkenderiFaruk Skenderi
Faruk Skenderi
JSJeffrey Swensen
Jeffrey Swensen
ZGZoran Gatalica
Zoran Gatalica
Spindle cell carcinoma is a rare subtype of metaplastic breast cancer, with triple-negative (TNBC: estrogen receptor-negative/progesterone receptor-negative/human epidermal growth factor receptor 2-negative) phenotype. It is associated with a marked resistance to conventional chemotherapy and has an overall poor outcome. Twenty-three pure spindle cell carcinomas of the breast (18 primary and 5 recurrent/metastatic) were comprehensively explored for biomarkers of immuno-oncology and targeted therapies using immunohistochemistry and DNA/RNA sequencing. The majority (21/23) of spindle cell carcinomas were TNBC. Estrogen and androgen receptor expression above the therapeutic thresholds were detected in 2 cases each. Pathogenic gene mutations were identified in 21 of 23 cases, including PIK3CA, TP53, HRAS, NF1, and PTEN. One case with matched pre- and post-chemotherapy samples exhibited a consistent mutational profile (PIK3CA and HRAS mutations) in both samples. Gene amplifications were present in 5 cases, including 1 case without detectable mutations. The spindle cell carcinomas cohort had consistently low total mutational burden (all below the 80th percentile for the entire TNBC cohort). All tumors were microsatellite stable. Programmed death-ligand 1 expression was observed on both tumor cells (in 7/21 cases), and in tumor-infiltrating immune cells (2/21 cases). Spindle cell carcinomas are characterized by targetable molecular alterations in the majority of cases, but owing to the lack of uniform findings, individual patient profiling is necessary. Detection of individual combinations of biomarkers should improve treatment options for this rare but aggressive disease.

1 February 2019 in Annals of Diagnostic Pathology
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Journal Article
Closed access
RTRobert Terlević
Robert Terlević
MBMelita Perić Balja
Melita Perić Balja
DTDavor Tomas
Davor Tomas
Faruk SkenderiFaruk Skenderi
Faruk Skenderi
BKBožo Krušlin
Božo Krušlin
ADAlma Demirovic
Alma Demirovic

15 September 2016 in Virchows Archiv
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Journal Article
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MFMaria Pané Foix
Maria Pané Foix
ADAna Dunatov
Ana Dunatov
PMPetr Martinek
Petr Martinek
EMEnric Condom Mundó
Enric Condom Mundó
SSSaul Suster
Saul Suster
Ondrej HesOndrej Hes
Ondrej Hes

27 February 2013 in Diagnostic Pathology
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Journal Article
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Faruk SkenderiFaruk Skenderi
Faruk Skenderi
FKFikreta Krakonja
Fikreta Krakonja
Semir VranicSemir Vranic
Semir Vranic
Introduction: Fibroadenomas are the most common benign breast tumors in young women. Infarction is rarely observed in fibroadenomas and when present, it is usually associated with pregnancy or lactation. Infarction can exceptionally occur as a complication of previous fine-needle aspiration biopsy or during lactation and pregnancy. Materials and methods: Retrospective review of 650 cases of fibroadenomas diagnosed at our institution during the 8-years period identified two cases of fibroadenomas with infarction (rate ~0.3%). Results: Two partially infarcted fibroadenomas were diagnosed on core biopsy and frozen section in an adolescent girl (13 years old) and in a young woman (25 years old), respectively. No preceding fine-needle aspiration biopsy was performed in these cases, nor were the patients pregnant or lactating at the time of the diagnosis. Conclusion: Spontaneous infarction within fibroadenoma is a rare phenomenon in younger patients. The presence of necrosis on core biopsy or frozen section should be cautiously interpreted and is not a sign of malignancy. Virtual Slides: The virtual slide(s) for this article can be found here:http://www.diagnosticpathology.diagnomx.eu/vs/1556060549847356