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High proliferation is associated with inferior Outcome in male breast cancer patients

Nilsson, Cecilia (författare)
Uppsala universitet,Centrum för klinisk forskning, Västerås,Institutionen för radiologi, onkologi och strålningsvetenskap,Vastmanland County Hospital, Sweden
Koliadi, Anthoula (författare)
Uppsala universitet,Enheten för onkologi,Uppsala University, Sweden
Johansson, Ida (författare)
Lund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,Lund University, Sweden
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Ahlin, Cecilia (författare)
Department of Oncology, Örebro University Hospital, Örebro, Sweden
Thorstenson, Sten (författare)
Linköpings universitet,Onkologi,Hälsouniversitetet,Department of Pathology, Linköping University Hospital, Linköping, Sweden
Bergkvist, Leif (författare)
Uppsala universitet,Centrum för klinisk forskning, Västerås,Vastmanland County Hospital, Sweden
Hedenfalk, Ingrid (författare)
Lund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,Lund University, Sweden
Fjällskog, Marie-Louise (författare)
Uppsala universitet,Enheten för onkologi,Uppsala University, Sweden
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 (creator_code:org_t)
Nature Publishing Group, 2013
2013
Engelska.
Ingår i: Modern Pathology. - : Nature Publishing Group. - 0893-3952 .- 1530-0285. ; 26:1, s. 87-94
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Assessment of proliferation is important in female breast cancer and individual treatment decisions are based upon its results, especially in the lumina! subgroups. Gene expression analyses fail to group male breast cancer into the intrinsic subgroups previously established in female breast cancer. Even though proliferation has been shown to divide male breast cancer into molecular subgroups with different prognoses, the clinical importance of proliferation markers has not yet been elucidated. Previous studies in male breast cancer have demonstrated contradictory results regarding the prognostic impact of histological grade and Ki-67, parameters strongly associated with proliferation. The aim of the present project was to study proliferation in male breast cancer by assessing other proliferation-related markers viz. cyclins A, B, D1 and mitotic count. A total of 197 male breast cancer cases with accessible paraffin-embedded material and outcome data were investigated. Immunohistochemical stainings were performed on tissue microarrays. Kaplan-Meier estimates and the Cox proportional regression models were used for survival analyses with breast cancer death as the event. The subset of patients with high expression of cyclin A (hazard ratio (HR) 3.7; P=0.001) and B (HR 2.7; P=0.02) demonstrated a poorer survival. Furthermore, high mitotic count was associated with an increased risk of breast cancer death (HR 2.5; P=0.01). In contrast, cyclin D1 overexpression was predictive of better breast cancer survival (HR 0.3; P=0.001). In conclusion, high levels of cyclin A and B expression and an elevated mitotic count result in a two to threefold higher risk for breast cancer death, whereas cyclin D1 overexpression halves the risk. The clinical utility of these proliferation markers needs further elucidation. Modern Pathology (2013) 26, 87-94; doi:10.1038/modpathol.2012.145; published online 24 August 2012

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

breast cancer
immunohistochemistry
male
MEDICINE
MEDICIN
breast cancer
immunohistochemistry
male

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