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. 2017 Oct;16(4):4634-4642.
doi: 10.3892/mmr.2017.7131. Epub 2017 Aug 2.

HPK1 positive expression associated with longer overall survival in patients with estrogen receptor-positive invasive ductal carcinoma‑not otherwise specified

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"V体育平台登录" HPK1 positive expression associated with longer overall survival in patients with estrogen receptor-positive invasive ductal carcinoma‑not otherwise specified

"V体育官网入口" Jiaojiao Wang et al. Mol Med Rep. 2017 Oct.

Abstract

Hematopoietic progenitor kinase 1 (HPK1) belongs to the mitogen activated protein kinase kinase kinase kinase (MAP4K) family of serine/threonine kinases, which have been associated with the incidence and progression of a variety of gastrointestinal malignant tumors in humans. However, the potential association between HPK1 expression and breast cancer, particularly invasive ductal carcinoma‑not otherwise specified (IDC‑NOS) development, has not yet been examined. To address this gap, the present study aimed to evaluate HPK1 expression in IDC‑NOS samples and to determine a relationship with clinical prognostic indicators, such as the expression levels of estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor 2 (HER2), as well as overall survival of the patients with IDC‑NOS. HPK1 mRNA and protein expression in samples from 148 patients with IDC‑NOS were detected using immunohistochemistry, western blotting and reverse transcription‑quantitative polymerase chain reaction. A total of 54 out of 148 (36. 5%) samples were HPK1‑positive, and 100 out of 148 (67. 6%) were ER‑positive. Of the latter, 28% (28/100) were HPK1‑positive, and a significant negative association of HPK1 expression with ER positivity was observed (P=0. 002; r=‑0. 254). In addition, 43. 2% (64/148) and 32. 4% (48/100) of IDC‑NOS tissues were PR‑ or HER2‑positive, respectively; however, neither indicator correlated with HPK1 (P=0. 109 and P=0. 558, respectively) VSports手机版. HPK1 expression, axillary lymph node metastasis and tumor‑node‑metastasis (TNM) stage were identified as independent factors of overall survival (OS) in the ER‑positive group (P<0. 05), and HPK1 positivity was associated with increased OS (P=0. 048). HPK1 mRNA levels did not differ between IDC‑NOS and normal adjacent breast tissues, whereas HPK1 protein levels were lower in IDC‑NOS (P<0. 05). These results suggested that HPK1 protein may be a potentially effective IDC-NOS therapeutic target. .

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Figures

Figure 1.
Figure 1.
Immunohistochemical staining of invasive ductal carcinoma-not otherwise specified tissues. Examples of positive and negative staining tissues are displayed; a positive signal was defined as the presence of a granular brown substance in the cytoplasm for HPK1, in the nucleus for ER and PR, and in the membrane for HER2. Magnification, ×400; scale bar=20 µm. ER, estrogen receptor; HER2, human epidermal growth factor receptor 2; HPK1, hematopoietic progenitor kinase 1; PR, progesterone receptor.
Figure 2.
Figure 2.
HPK1 mRNA expression levels in IDC-NOS tissues and adjacent paired NATs. HPK1 mRNA expression levels in the IDC-NOS group were 0.9836±0.1268. No significant differences were identified following reverse transcription-quantitative polymerase chain reaction analysis (P>0.05). Data are presented as the mean ± standard deviation. HPK1, hematopoietic progenitor kinase 1; IDC-NOS, invasive ductal carcinoma-not otherwise specified tissues; NAT, normal adjacent tissue.
Figure 3.
Figure 3.
HPK1 protein expression in ER-positive IDC-NOS tissues and paired normal tissues. Western blot analysis was used to determine the HPK1 protein expression levels in tissue samples of 20 patients randomly selected from the ER-positive IDC-NOS group; the bar graph represents the densitometric analysis normalized to β-actin. (A) The average HPK1 protein expression levels of these 20 patients were as follows: NAT, 0.302±0.018; IDC-NOS, 0.1453±0.018. *P<0.05 vs. IDC-NOS. (B) A total of 4 of these 20 patients were randomly chosen and are presented in the figure as a representation of the results. *P<0.05 and **P<0.01 vs. c tissues. Data are presented as the mean ± standard deviation. c, cancerous tissue; ER, estrogen receptor; HPK1, hematopoietic progenitor kinase 1; IDC-NOS, invasive ductal carcinoma-not otherwise specified tissues; n, normal adjacent tissue.
Figure 4.
Figure 4.
HPK1 expression and overall survival. Kaplan-Meier analysis of survival among patients with estrogen receptor-positive invasive ductal carcinoma-not otherwise specified. HPK1, hematopoietic progenitor kinase 1; censored, mortality.

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