Burhan Abdullah Zaman

Dr. Burhan Abdullah Zaman

University of Duhok, Dihok, Iraq
orcid

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

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

Representative Publications

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3 January 2022 in Cancer Cell International
Verified
Journal Article
Open access
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Somayeh VafaeiSomayeh Vafaei
Somayeh Vafaei
AZAngelina O. Zekiy
Angelina O. Zekiy
RKRamadhan Ado Khanamir
Ramadhan Ado Khanamir
Burhan Abdullah ZamanBurhan Abdullah Zaman
Burhan Abdullah Zaman
AGArman Ghayourvahdat
Arman Ghayourvahdat
MZMajid Zamani
Majid Zamani
Recently, immune checkpoint inhibitors (ICIs) therapy has become a promising therapeutic strategy with encouraging therapeutic outcomes due to their durable anti-tumor effects. Though, tumor inherent or acquired resistance to ICIs accompanied with treatment-related toxicities hamper their clinical utility. Overall, about 60–70% of patients (e.g., melanoma and lung cancer) who received ICIs show no objective response to intervention. The resistance to ICIs mainly caused by alterations in the tumor microenvironment (TME), which in turn, supports angiogenesis and also blocks immune cell antitumor activities, facilitating tumor cells' evasion from host immunosurveillance. Thereby, it has been supposed and also validated that combination therapy with ICIs and other therapeutic means, ranging from chemoradiotherapy to targeted therapies as well as cancer vaccines, can capably compromise tumor resistance to immune checkpoint blocked therapy. Herein, we have focused on the therapeutic benefits of ICIs as a groundbreaking approach in the context of tumor immunotherapy and also deliver an overview concerning the therapeutic influences of the addition of ICIs to other modalities to circumvent tumor resistance to ICIs.

8 January 2022 in Current Problems in Cardiology
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Journal Article
Closed access
RDRumi Iqbal Doewes
Rumi Iqbal Doewes
GGGhazal Gharibian
Ghazal Gharibian
FZFiroozeh Abolhasani Zadeh
Firoozeh Abolhasani Zadeh
Burhan Abdullah ZamanBurhan Abdullah Zaman
Burhan Abdullah Zaman
SVSahar Vahdat
Sahar Vahdat
RAReza Akhavan-Sigari
Reza Akhavan-Sigari

8 May 2022 in Stem Cell Research & Therapy
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Journal Article
Open access
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SSSamin Shokravi
Samin Shokravi
VBVitaliy Borisov
Vitaliy Borisov
Burhan Abdullah ZamanBurhan Abdullah Zaman
Burhan Abdullah Zaman
FNFiroozeh Niazvand
Firoozeh Niazvand
RHRaheleh Hazrati
Raheleh Hazrati
AZAmir Zamani
Amir Zamani
Recently, mesenchymal stromal cells (MSCs) and their derivative exosome have become a promising approach in the context of liver diseases therapy, in particular, acute liver failure (ALF). In addition to their differentiation into hepatocytes in vivo, which is partially involved in liver regeneration, MSCs support liver regeneration as a result of their appreciated competencies, such as antiapoptotic, immunomodulatory, antifibrotic, and also antioxidant attributes. Further, MSCs-secreted molecules inspire hepatocyte proliferation in vivo, facilitating damaged tissue recovery in ALF. Given these properties, various MSCs-based approaches have evolved and resulted in encouraging outcomes in ALF animal models and also displayed safety and also modest efficacy in human studies, providing a new avenue for ALF therapy. Irrespective of MSCs-derived exosome, MSCs-based strategies in ALF include administration of native MSCs, genetically modified MSCs, pretreated MSCs, MSCs delivery using biomaterials, and also MSCs in combination with and other therapeutic molecules or modalities. Herein, we will deliver an overview regarding the therapeutic effects of the MSCs and their exosomes in ALF. As well, we will discuss recent progress in preclinical and clinical studies and current challenges in MSCs-based therapies in ALF, with a special focus on in vivo reports.

4 May 2022 in Cellular & Molecular Biology Letters
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Journal Article
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SBSadegh Shojaei Baghini
Sadegh Shojaei Baghini
ZGZhanna Gardanova
Zhanna Gardanova
SASaeme Azizi Hassan Abadi
Saeme Azizi Hassan Abadi
Burhan Abdullah ZamanBurhan Abdullah Zaman
Burhan Abdullah Zaman
AIAhmet İlHan
Ahmet İlHan
AYAmirhossein Fakhre Yaseri
Amirhossein Fakhre Yaseri
The progress of genetic engineering in the 1970s brought about a paradigm shift in genome editing technology. The clustered regularly interspaced short palindromic repeats/CRISPR associated protein 9 (CRISPR/Cas9) system is a flexible means to target and modify particular DNA sequences in the genome. Several applications of CRISPR/Cas9 are presently being studied in cancer biology and oncology to provide vigorous site-specific gene editing to enhance its biological and clinical uses. CRISPR's flexibility and ease of use have enabled the prompt achievement of almost any preferred alteration with greater efficiency and lower cost than preceding modalities. Also, CRISPR/Cas9 technology has recently been applied to improve the safety and efficacy of chimeric antigen receptor (CAR)-T cell therapies and defeat tumor cell resistance to conventional treatments such as chemotherapy and radiotherapy. The current review summarizes the application of CRISPR/Cas9 in cancer therapy. We also discuss the present obstacles and contemplate future possibilities in this context.

1 July 2019 in The Journal of Maternal-Fetal & Neonatal Medicine
Verified
Journal Article
Closed access
Burhan Abdullah ZamanBurhan Abdullah Zaman
Burhan Abdullah Zaman
SRSuzan Rasool
Suzan Rasool
SJSaja Jasim
Saja Jasim
Deldar Morad AbdulahDeldar Morad Abdulah
Deldar Morad Abdulah
Objectives: Hepcidin hormone production is suppressed in the case of iron deficiency. The role of hepcidin as a hormone in iron metabolism along with its diagnostic cut-off values and its sensitivity and specificity among pregnant women with iron deficiency anemia was examined in this study. Methods: In this case-control study, three groups of pregnant subjects were included according to the following criteria: cases/Patient group: pregnant women with iron deficiency anemia based on, Hb < 11.5 g/dl, S ferritin < 10 ng/ml, TS% < 15%; positive control group: pregnant women with noniron deficiency anemia based on, Hb < 11.5 g/dl, S ferritin > 10 ng/ml, TS% > 15%; and negative control group: included nonanemic apparently healthy pregnant women based on, Hb > 11.5 g/dl, S ferritin > 10 ng/ml, TS% > 15%. Results: The serum hepcidin was significantly lower in pregnant women with iron deficiency anemia (0.34 ng/ml) compared to its level in pregnant women with noniron deficiency anemia (23.48 ng/l) and apparently healthy pregnant women (13.86 ng/ml; p < 0.001). The study found a significant correlation between serum hepcidin and iron deficiency-related parameters with adjustment for study groups (p < 0.01). Moreover, the study found that serum hepcidin has good sensitivity in the range of 0.49–0.76 ng/ml (80.6–83.3%) and good specificity (76.2%) over positive iron deficiency anemia. Similar results were found for serum hepcidin over negative control group (0.49–0.83 ng/ml; sensitivity: 80.6–83.3%; specificity: 75.8–78.8%). Conclusion: This study suggests that serum hepcidin is superior to hemoglobin, serum iron, serum ferritin, TS, and TIBC as an indicator of iron deficiency anemia in pregnant women.

25 July 2024 in ARO-THE SCIENTIFIC JOURNAL OF KOYA UNIVERSITY
Verified
Journal Article
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Deldar Morad AbdulahDeldar Morad Abdulah
Deldar Morad Abdulah
Burhan Abdullah ZamanBurhan Abdullah Zaman
Burhan Abdullah Zaman
ZMZuhair Rushdi Mustafa
Zuhair Rushdi Mustafa
LHLokman H. Hassan
Lokman H. Hassan
This study investigates the use of artificial intelligence (AI) technologies among academics at the University of Duhok (UoD), focusing on their perspectives, preferences, and intentions toward integrating AI within academic and research environments. A survey was conducted through Google Forms, targeting postgraduate students, recent alumni (since 2020), and faculty members of UoD in the Kurdistan region of Iraq. A total of 674 participants, aged 22–70 years, responded. The findings indicate that only 36.94% had employed AI technologies. Among AI users (n = 249), primary sources of information were friends or colleagues (46.59%) and social media (35.74%). Younger individuals and those holding master’s degrees exhibited a stronger tendency toward AI usage (p < 0.0001), whereas gender and academic discipline had minimal influence. ChatGPT was the most widely used tool (70.68%), followed by Quill Bot (42.17%), Grammarly (34.94%), and Google Bard (29.32%). The main AI applications were text paraphrasing (33.73%) and information retrieval (15.26%). Notably, 47.58% of respondents recommended AI for various academic tasks, including scientific research and idea generation. In conclusion, the study shows that only one-third of UoD faculty members utilize AI, predominantly for text paraphrasing. Nearly half of the participants suggested the adoption of AI by postgraduate students and academic staff.