Anja Rieger

Dr. Anja Rieger


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

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

Representative Publications

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1 August 2019 in Clinical Nutrition
Verified
Journal Article
Closed access
SPSophie Pevny
Sophie Pevny
SMSebastian Maasberg
Sebastian Maasberg
ARAnja Rieger
Anja Rieger
MKMirjam Karber
Mirjam Karber
EBElisabeth Blüthner
Elisabeth Blüthner
UPUlrich-Frank Pape
Ulrich-Frank Pape

Verified
Journal Article
Open access
PDF file
IKIlka Kristiansen
Ilka Kristiansen
Carsten StephanCarsten Stephan
Carsten Stephan
KJKlaus Jung
Klaus Jung
MDManfred Dietel
Manfred Dietel
ARAnja Rieger
Anja Rieger
GKGlen Kristiansen
Glen Kristiansen
Aims: Determining the origin of metastases is an important task of pathologists to allow for the initiation of a tumor-specific therapy. Recently, homeobox protein Hox-B13 (HOXB13) has been suggested as a new marker for the detection of prostatic origin. The aim of this study was to evaluate the diagnostic sensitivity of HOXB13 in comparison to commonly used immunohistochemical markers for prostate cancer. Materials and methods: Histologically confirmed prostate cancer lymph node metastases from 64 cases were used to test the diagnostic value of immunohistochemical markers: prostate specific antigen (PSA), Prostatic acid phosphatase (PSAP), prostate specific membrane antigen (PSMA), homeobox gene NKX3.1, prostein, androgen receptor (AR), HOXB13, and ETS-related gene (ERG). All markers were evaluated semi-quantitatively using Remmele's immune reactive score. Results: The detection rate of prostate origin of metastasis for single markers was 100% for NKX3.1, 98.1% for AR, 84.3% for PSMA, 80.8% for PSA, 66% for PSAP, 60.4% for HOXB13, 59.6% for prostein, and 50.0% for ERG. Conclusions: Our data suggest that HOXB13 on its own lacks sensitivity for the detection of prostatic origin. Therefore, this marker should be only used in conjunction with other markers, preferably the highly specific PSA. The combination of PSA with NKX3.1 shows a higher sensitivity and thus appears preferable in this setting.