Zakaria Einbeigi

Dr. Zakaria Einbeigi


Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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2 January 2013 in BMC Cancer
Verified
Journal Article
Open access
PDF file
ESEmman Shubbar
Emman Shubbar
AKAnikó Kovács
Anikó Kovács
SHShahin Hajizadeh
Shahin Hajizadeh
TPToshima Z Parris
Toshima Z Parris
SNSzilard Nemes
Szilard Nemes
Khalil HelouKhalil Helou
Khalil Helou
Breast cancer is a potentially fatal malignancy in females despite the improvement in therapeutic techniques. The identification of novel molecular signatures is needed for earlier detection, monitoring effects of treatment, and predicting prognosis. We have previously used microarray analysis to identify differentially expressed genes in aggressive breast tumors. The purpose of the present study was to investigate the prognostic value of the candidate biomarkers CCNB2, ASPM, CDCA7, KIAA0101, and SLC27A2 in breast cancer.

1 February 2013 in BMC Cancer
Verified
Journal Article
Open access
PDF file
ESEmman Shubbar
Emman Shubbar
Khalil HelouKhalil Helou
Khalil Helou
AKAnikó Kovács
Anikó Kovács
SNSzilard Nemes
Szilard Nemes
SHShahin Hajizadeh
Shahin Hajizadeh
ZEZakaria Einbeigi
Zakaria Einbeigi
Previously, we performed analysis of gene expression in 46 axillary lymph node negative tumors and identified molecular gene signatures that resulted in different clinical outcomes. The aim of this study was to determine the correlation of γ-glutamyl hydrolase (GGH), fatty acid amide hydrolase (FAAH), Pirin (PIR) and TAF5-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor, 65 kDa (TAF5L), selected from identified gene signatures, with clinical outcomes as well as classical clinicopathological characteristics in primary invasive breast cancer patients.

4 May 2021 in Cancers
Verified
Journal Article
Open access
PDF file
NONina Oparina
Nina Oparina
MEMalin C Erlandsson
Malin C Erlandsson
ABAnna Fäldt Beding
Anna Fäldt Beding
TPToshima Z Parris
Toshima Z Parris
Khalil HelouKhalil Helou
Khalil Helou
Maria I BokarewaMaria I Bokarewa
Maria I Bokarewa
Breast cancer (BC) histological and molecular classifications significantly improved the treatment strategy and prognosis. Inhibitor of apoptosis BIRC5/survivin is often overexpressed in cancers, however, indications of its importance in BC are inconsistent. We integrate BIRC5 protein and mRNA measures with clinical associates and long-term outcome in three independent cohorts Protein levels of BIRC5 were measured in primary lysates of 845 patients of the West Swedish BC cohort (VGR-BC) and linked to 5- and 27-years survival. The results were externally validated in transcriptomic data from METABRIC and SCAN-B cohorts. Survival analysis showed that high levels of BIRC5 were consistently associated with a poor probability of 5-year overall survival. High BIRC5 in VGR-BC contributed negatively to the disease-specific survival at 5 and 27 years. Subsets with different status by ER (estrogen receptor) expression and presence of nodal metastasis supported independent association of high BIRC5 with poor prognosis in all cohorts. In METABRIC and SCAN-B cohorts, high levels of BIRC5 mRNA were associated with the basal-like and luminal B molecular BC subtypes and with increasing histologic grade. BIRC5 is a sensitive survival marker that acts independent of ER and nodal status, and its levels need to be considered when making treatment decisions.

1 October 2001 in European Journal of Cancer
Verified
Journal Article
Closed access
ZEZakaria Einbeigi
Zakaria Einbeigi
ABA Bergman
A Bergman
LKL.-G Kindblom
L.-G Kindblom
TMTommy Martinsson
Tommy Martinsson
JMJ.M Meis-Kindblom
J.M Meis-Kindblom
PKP Karlsson
P Karlsson

31 August 2006 in Familial Cancer
Verified
Journal Article
Closed access
PDF file
ZEZakaria Einbeigi
Zakaria Einbeigi
ABAnnika Bergman
Annika Bergman
JMJeanne M. Meis-Kindblom
Jeanne M. Meis-Kindblom
AFAnna Flodin
Anna Flodin
CBCecilia Bjursell
Cecilia Bjursell
PKPer Karlsson
Per Karlsson

16 December 2019 in Genes
Verified
Journal Article
Open access
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AÖanna öfverholm
anna öfverholm
ZEZakaria Einbeigi
Zakaria Einbeigi
AWAntonia Wigermo
Antonia Wigermo
EHErik Holmberg
Erik Holmberg
PKPer Karlsson
Per Karlsson
Women with BRCA variants have a high lifetime risk of developing breast and ovarian cancer. The aim of this study was to investigate the standard incidence ratios (SIR) for breast and ovarian cancer and standard mortality ratios (SMR) in a population-based cohort of women in Western Sweden, under surveillance and after risk reducing surgery. Women who tested positive for a BRCA variant between 1995–2016 (n = 489) were prospectively registered and followed up for cancer incidence, risk reducing surgery and mortality. The Swedish Cancer Register was used to compare breast and ovarian cancer incidence and mortality with and without risk reducing surgery for women with BRCA variants in comparison to women in the general population. SIR for breast cancer under surveillance until risk-reducing mastectomy (RRM) was 14.0 (95% CI 9.42–20.7) and decreased to 1.93 (95% CI 0.48–7.7) after RRM. The SIR for ovarian cancer was 124.6 (95% CI 59.4–261.3) under surveillance until risk reducing salpingo-oophorectomy (RRSO) and decreased to 13.5 (95% CI 4.34–41.8) after RRSO. The SMR under surveillance before any risk reducing surgery was 5.56 (95% 2.09–14.8) and after both RRM and RRSO 4.32 (95% CI 1.62–11.5). Women with cancer diagnoses from the pathology report after risk reducing surgery were excluded from the analyses. Risk reducing surgery reduced the incidence of breast and ovarian cancer in women with BRCA variants. However, overall mortality was significantly increased in comparison to the women in the general population and remained elevated even after risk reducing surgery. These findings warrant further research regarding additional measures for these women.