Arko-Boham Benjamin, Lomotey Justice Tanihu, Tetteh Emmanuel Nomo, Tagoe Emmanuel Ayitey, Aryee Nii Ayite, Owusu Ewurama Ampadu, Okai Isaac, Blay Richard Michael, Clegg-Lamptey Joe-Nat
Department of Medical Laboratory Sciences, School of Biomedical and Allied Health Sciences, College of Health Sciences, University of Ghana, Korle-Bu, Accra, Ghana.
West African Centre for Cell Biology of Infectious Pathogens, University of Ghana, Legon, Accra, Ghana.
Biomark Res. 2017 Jun 9;5:21. doi: 10.1186/s40364-017-0100-0. eCollection 2017.
Breast cancer, the most commonly diagnosed cancer among women and leading cause of cancer-related deaths worldwide, exhibits aggressive behavior in indigenous African women evidenced by high histologic grade tumours with low hormone receptor positivity. Aggressive breast cancers grow quickly, easily metastasize and recur and often have unfavourable outcomes. The current study investigated candidate genes that may regulate tumour aggression in Ghanaian women. We hypothesize that increased expression and function of certain genes other than the widely-held view attributing breast cancer aggression in African populations to their younger population age may be responsible for the aggressive nature of tumours.
Employing ELISA, we assayed for vimentin and death-associated protein kinase 1 (DAPK1) from thawed archived (stored at -80 °C) serum samples obtained from 40 clinically confirmed Ghanaian breast cancer patients and 40 apparently healthy controls. Patients' clinical records and tumour parameters matching the samples were retrieved from the database of the hospital. ANOVA was used to compare means of serum protein concentration among groups while Chi-square analysis was used for the categorical data sets with -value ≤0.05 considered significant. Multiple logistic regression analysis was conducted to determine the association between protein concentration and tumour parameters.
Of the 80 samples, 27 (33.8%) and 53 (66.2%) were from young (<35 years) and old (≥35 years), respectively. Vimentin and DAPK1 concentration were higher in patients than controls with higher levels in "young" age group than "old" age group. Vimentin concentration was highest in grade 3 tumours followed by grade 2 and 1 but that for DAPK1 was not significant. For vimentin, tumour area strongly correlated with tumour grade ( = 0.696, < 0.05) but weakly correlated with tumour stage ( = 0.420, < 0.05). Patient's age correlated with DAPK1 concentration ( = 0.393, < 0.05). DAPK1 serum levels weakly correlated with cancer duration ( = 0.098, = 0.27) and tumour size ( = 0.40, < 0.05).
Serum concentration of Vimentin and DAPK1 are elevated in Ghanaian breast cancer patients. This may be partly responsible for aggressive nature of the disease among the population. Vimentin and DAPK1 should be explored further as potential breast cancer biomarkers in Africans.
乳腺癌是女性中最常被诊断出的癌症,也是全球癌症相关死亡的主要原因。在非洲本土女性中,乳腺癌表现出侵袭性,其组织学分级高且激素受体阳性率低。侵袭性乳腺癌生长迅速,容易转移和复发,且往往预后不佳。本研究调查了可能调节加纳女性肿瘤侵袭性的候选基因。我们假设,除了普遍认为非洲人群中乳腺癌侵袭性是由于其较年轻的年龄外,某些基因表达和功能的增加可能是肿瘤具有侵袭性的原因。
我们采用酶联免疫吸附测定法(ELISA),对从40例临床确诊的加纳乳腺癌患者和40例明显健康的对照者身上获取的解冻后的存档血清样本(保存在-80°C)进行波形蛋白和死亡相关蛋白激酶1(DAPK1)检测。从医院数据库中检索与样本匹配的患者临床记录和肿瘤参数。采用方差分析比较各组血清蛋白浓度的均值,而卡方分析用于分类数据集,P值≤0.05被认为具有统计学意义。进行多因素逻辑回归分析以确定蛋白浓度与肿瘤参数之间的关联。
在这80个样本中,分别有27个(33.8%)和53个(66.2%)来自年轻(<35岁)和年长(≥35岁)的患者。患者的波形蛋白和DAPK1浓度高于对照组,且“年轻”年龄组的水平高于“年长”年龄组。波形蛋白浓度在3级肿瘤中最高,其次是2级和1级,但DAPK1浓度差异无统计学意义。对于波形蛋白,肿瘤面积与肿瘤分级密切相关(r = 0.696,P < 0.05),但与肿瘤分期弱相关(r = 0.420,P < 0.05)。患者年龄与DAPK1浓度相关(r = 0.393,P < 0.05)。DAPK1血清水平与癌症病程弱相关(r = 0.098,P = 0.27),与肿瘤大小弱相关(r = 0.40,P < 0.05)。
加纳乳腺癌患者血清中波形蛋白和DAPK1浓度升高。这可能部分是该人群中疾病具有侵袭性的原因。波形蛋白和DAPK1应作为非洲人潜在的乳腺癌生物标志物进一步研究。