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      HER—4在結(jié)直腸癌中的表達(dá)及其臨床意義

      2017-06-01 15:40:16劉傳淵夏來(lái)陽(yáng)劉金秀王建
      中國(guó)現(xiàn)代醫(yī)生 2016年34期
      關(guān)鍵詞:靶點(diǎn)直腸癌染色

      劉傳淵 夏來(lái)陽(yáng) 劉金秀 王建

      [摘要] 目的 研究HER-4蛋白在結(jié)直腸癌中的表達(dá),并探討其臨床意義。 方法 采用免疫組織化學(xué)Envision二步法檢測(cè)100例患者結(jié)直腸癌組織、20例正常癌旁組織中HER-4蛋白的表達(dá),分析HER-4蛋白表達(dá)水平與臨床病理因素間的關(guān)系。 結(jié)果 HER-4蛋白在正常癌旁組織、結(jié)直腸癌中的表達(dá)率分別為0%、44%,差異有統(tǒng)計(jì)學(xué)意義(P=0.000),結(jié)直腸癌組織中HER-4蛋白表達(dá)與淋巴結(jié)轉(zhuǎn)移、TNM分期密切相關(guān)(P<0.05),而與性別、年齡、腫瘤部位、腫瘤大體、病理類(lèi)型、浸潤(rùn)深度、脈管癌栓、術(shù)前癌胚抗原(CEA)等無(wú)關(guān)。 結(jié)論 HER-4蛋白在結(jié)直腸正常癌旁組織中未見(jiàn)陽(yáng)性表達(dá),而在結(jié)直腸癌病灶中呈現(xiàn)高表達(dá),且與淋巴結(jié)轉(zhuǎn)移、TNM分期密切相關(guān),高表達(dá)者預(yù)示病程較晚,預(yù)后較差。HER-4不僅是一個(gè)有價(jià)值的生物標(biāo)志物,而且是一個(gè)潛在的抗癌治療靶點(diǎn)。

      [關(guān)鍵詞] 基因;HER-4;腫瘤;結(jié)直腸;免疫組織化學(xué);病理學(xué)

      [中圖分類(lèi)號(hào)] R735.3 [文獻(xiàn)標(biāo)識(shí)碼] A [文章編號(hào)] 1673-9701(2016)34-0013-04

      Expressions and clinical significance of HER-4 in colorectal cancer

      LIU Chuanyuan1 XIA Laiyang1 LIU Jinxiu2 WANG Jian3

      1.Department of No.1 General Surgery, Ganzhou People's Hospital in Jiangxi Province, Ganzhou 341000, China; 2.The Second Affiliated Hospital of Gannan Medical College,Ganzhou 341600, China; 3.Department of Pathology, Ganzhou People's Hospital in Jiangxi Province, Ganzhou 341000, China

      [Abstract] Objective To evaluate the HER-4 expression and its correlation with clinical pathological parameters in colorectal cancer patients. Methods The expressions of HER-4 protein in 100 cases of colorectal carcinoma and 20 cases of normal colorectal tissues were detected by immunohistochemistry method, and the association between the expression and the clinicopathological parameter of colorectal carcinoma was analyzed. Results Positive staining of HER-4 was observed in 44% colorectal cancer tissues compared with 0% in normal colorectal epithelia(P=0.000). HER-4 expression was associated with lymph node metastasis and TNM stage(P<0.05), and was not correlated with age, gender, tumor location, tumor gross, pathological type, tumor depth, invasion of vessel and preoperative serum carcinoembryonic antigen(CEA). Conclusion HER-4 protein expression in colorectal normal tissue was negative, but in colorectal cancer lesions showed high, which was closely related to lymph node metastasis and TNM stage. High expression indicates a late course of disease, and a poor prognosis. HER-4 is not only a valuable biomarker, but also a potential therapeutic target in colorectal cancer.

      [Key words] Gene; HER-4; NeopIasms; Colorectum; Immunohistochemistry; Pathology

      過(guò)去的幾十年中,結(jié)直腸癌的發(fā)病率和死亡率在許多地區(qū)已顯著增加[1,2]。在美國(guó),2014年新發(fā)結(jié)直腸癌病約為136 830例,近50 310的患者死于該疾病[3]。根治手術(shù)后5年生存率約為60%[4-6]。為了改善結(jié)直腸癌的預(yù)后,隨著精準(zhǔn)醫(yī)療的推進(jìn),尋找有效的治療靶點(diǎn)具有重要的意義。人表皮生長(zhǎng)因子受體(HER)家族包括EGFR(HER-1)、HER-2、HER-3和 HER-4,它們是具有典型的胞外受體結(jié)合位點(diǎn)的酪氨酸激酶受體。HER激活多條信號(hào)傳導(dǎo)通路并且通過(guò)此環(huán)節(jié)影響大量的信號(hào)傳導(dǎo)過(guò)程,這些受體的異常激活與不同的病理過(guò)程密切相關(guān),影響腫瘤的增殖、分化和轉(zhuǎn)移。HER-1過(guò)度表達(dá)在許多癌癥中提示預(yù)后不良[7,8],HER-2在乳腺癌和胃癌診療中已經(jīng)成為重要的生物標(biāo)志物和治療靶點(diǎn)[9,10]。HER-3的表達(dá)與實(shí)體腫瘤預(yù)后差明顯相關(guān)[11]。HER-4對(duì)腫瘤的作用仍存在爭(zhēng)議,有報(bào)道認(rèn)為在宮頸癌中與更好的預(yù)后有關(guān)[12],同時(shí)也有報(bào)道認(rèn)為在口腔鱗狀細(xì)胞癌中HER-4蛋白的過(guò)表達(dá)提示遠(yuǎn)處轉(zhuǎn)移和更差的生存預(yù)后[13]。HER-4在結(jié)直腸癌中的研究甚少,HER-4在結(jié)直腸癌中的作用如何,能否作為一個(gè)潛在的治療靶點(diǎn)?本研究就HER-4在結(jié)直腸癌中的表達(dá)進(jìn)行研究,并分析其與臨床病理間的關(guān)系。

      1 資料與方法

      1.1 一般資料

      選取2014年7月~2015年7月我院胃腸外科行根治性手術(shù)的結(jié)直腸癌患者標(biāo)本100例,術(shù)前均未行新輔助放、化療。其中男52例,女48例;年齡26~81歲,中位年齡62歲;結(jié)腸癌49例、直腸癌51例。依據(jù)患者年齡、性別、腫瘤部位、腫瘤大小、淋巴結(jié)轉(zhuǎn)移、TNM分期等進(jìn)行分組(表1)。另取20例癌旁正常組織作為對(duì)照組。

      1.2 免疫組織化學(xué)染色

      鼠抗人單克隆HER-4抗體(克隆號(hào) HFR1-ab 1939,工作濃度1:100)購(gòu)自Abcam香港有限公司。Envision反應(yīng)液購(gòu)自福建邁新公司。采用免疫組織化學(xué)Envision二步法檢測(cè)HER-4在結(jié)直腸癌中的表達(dá),組織石蠟切片經(jīng)脫蠟、水化、自來(lái)水沖洗,并對(duì)組織行高壓抗原修復(fù),實(shí)驗(yàn)步驟按照試劑盒進(jìn)行。實(shí)驗(yàn)同時(shí)設(shè)陽(yáng)性對(duì)照(已知陽(yáng)性的腎組織切片)和陰性對(duì)照(PBS代替一抗)。

      1.3評(píng)定標(biāo)準(zhǔn)

      對(duì)結(jié)果進(jìn)行雙盲閱片。HER-4定位于細(xì)胞膜或細(xì)胞核,染色判讀及評(píng)分參照Lai C、Kountourskis P等[14,18]的研究標(biāo)準(zhǔn):(0):不染色或<10%腫瘤細(xì)胞染色;(1+):>10%的腫瘤細(xì)胞微弱或隱約可見(jiàn)染色;(2+):>10%的腫瘤細(xì)胞弱到中度染色;(3+):>10%的腫瘤細(xì)胞強(qiáng)染色。(0)和(1+)定義為低表達(dá)(陰性表達(dá)),(2+)和(3+)定義為高表達(dá)(陽(yáng)性表達(dá))。

      1.4 統(tǒng)計(jì)學(xué)處理

      使用SPSS 19.0統(tǒng)計(jì)學(xué)軟件對(duì)數(shù)據(jù)進(jìn)行分析,計(jì)數(shù)資料采用χ2檢驗(yàn)、四格表Fishers確切概率法,P<0.05為差異有統(tǒng)計(jì)學(xué)意義。

      2 結(jié)果

      2.1 結(jié)直腸癌組織、正常結(jié)直腸癌旁組織中HER-4表達(dá)情況

      HER-4蛋白主要表達(dá)于癌組織細(xì)胞膜或細(xì)胞核中(圖1、2),HER-4在結(jié)直腸癌組織中的陽(yáng)性表達(dá)率為44%(44/100),而在20例正常癌旁組織中未見(jiàn)表達(dá),二者陽(yáng)性表達(dá)率差異有統(tǒng)計(jì)學(xué)意義(P=0.000)(表1)。

      2.2 結(jié)直腸癌組織中HER-4表達(dá)情況與臨床病理因素的關(guān)系

      HER-4蛋白在結(jié)直腸癌組織中的表達(dá)程度與淋巴結(jié)轉(zhuǎn)移、TNM分期有關(guān)(P<0.05),與患者性別、年齡、腫瘤部位、腫瘤大體、病理類(lèi)型、浸潤(rùn)層次、脈管癌栓、術(shù)前癌胚抗原(CEA)、術(shù)前糖類(lèi)抗原199(CA199)等無(wú)關(guān)(表2)。

      3 討論

      HER-4基因是HER癌基因家族的一員,首次被發(fā)現(xiàn)是在小鼠神經(jīng)系統(tǒng)發(fā)育的研究中,其在小鼠神經(jīng)系統(tǒng)發(fā)育階段呈現(xiàn)廣泛表達(dá)[15],后來(lái)發(fā)現(xiàn)正常的人體腦組織、骨骼肌、心肌和垂體組織中也有不同的表達(dá),在多種腫瘤組織中存在過(guò)度表達(dá)[16-18]。本研究中,HER-4蛋白在正常結(jié)直腸黏膜組織中未見(jiàn)陽(yáng)性表達(dá),而在結(jié)直腸癌病灶中呈現(xiàn)高表達(dá),此與有關(guān)研究的結(jié)論類(lèi)似[14,19-20]。

      淋巴結(jié)轉(zhuǎn)移是影響結(jié)直腸癌術(shù)后生存最重要的因素之一,也是腫瘤分期及術(shù)后進(jìn)一步綜合治療的重要依據(jù),淋巴結(jié)轉(zhuǎn)移預(yù)示著病程較晚,預(yù)后較差。本研究結(jié)果顯示,HER-4在結(jié)直腸癌原發(fā)灶中的陽(yáng)性表達(dá)率為44%(44/100),存在高表達(dá);與結(jié)直腸癌淋巴結(jié)轉(zhuǎn)移有關(guān)(P=0.039),淋巴結(jié)轉(zhuǎn)移者陽(yáng)性表達(dá)率明顯高于無(wú)淋巴結(jié)轉(zhuǎn)移者。這與Kountourskis等[18]的研究結(jié)果相同,其對(duì)106個(gè)結(jié)直腸腫瘤組織進(jìn)行免疫組化,結(jié)果發(fā)現(xiàn)HER-4表達(dá)陽(yáng)性與患者的淋巴結(jié)轉(zhuǎn)移相關(guān)(P=0.01),HER-4的高表達(dá)與癌細(xì)胞的轉(zhuǎn)移能力密切相關(guān)。Baiocchi G等[20]認(rèn)為HER-4表達(dá)陽(yáng)性是淋巴結(jié)轉(zhuǎn)移、腫瘤復(fù)發(fā)的一個(gè)獨(dú)立危險(xiǎn)因素。

      在國(guó)際抗癌聯(lián)盟(UICC)、美國(guó)癌癥聯(lián)合委員會(huì)(AJCC)的共同努力推動(dòng)下,原發(fā)腫瘤一區(qū)域淋巴結(jié)一遠(yuǎn)處轉(zhuǎn)移(TNM)分期系統(tǒng)不斷完善,逐步成為全球腫瘤研究工作者比較各自臨床資料、評(píng)價(jià)治療效果的共同依據(jù)。TNM分期越后,其預(yù)后越差。本研究中,TNM分期Ⅰ、Ⅱ、Ⅲ期患者其HER-4表達(dá)率分別為9.31%、38.82%、51.87%,差異具統(tǒng)計(jì)學(xué)意義(P=0.042),提示HER-4的表達(dá)與TNM分期密切相關(guān),分期越后,原發(fā)腫瘤病灶中其HER-4表達(dá)越高。這與一些學(xué)者的研究結(jié)果類(lèi)似。Lee JC等[19]發(fā)現(xiàn)結(jié)直腸癌TNM分期Ⅰ或Ⅱ期腫瘤病灶HER-4陽(yáng)性表達(dá)明顯低于Ⅲ或Ⅳ期腫瘤病灶,He XX等[21]發(fā)現(xiàn)HER-4在胃癌中的表達(dá)與腫瘤的TNM分期密切相關(guān)。腫瘤是多基因、多因素長(zhǎng)期共同作用的結(jié)果,HER-4陽(yáng)性表達(dá)率越高,預(yù)示分期越晚。有學(xué)者報(bào)道,在人肺癌細(xì)胞 H1299中轉(zhuǎn)染入HER-4,與對(duì)照組相比,HER-4明顯促進(jìn)了肺癌細(xì)胞的生長(zhǎng),而使用抗HER-4的抗體Mab-3之后,發(fā)現(xiàn)表達(dá)HER-4的肺癌細(xì)胞不僅生長(zhǎng)速度明顯受到抑制,而且凋亡速度顯著加快[22]。通過(guò)敲除、下調(diào)HER-4的表達(dá),能抑制腫瘤細(xì)胞的增值與生長(zhǎng)[23]。

      綜上所述,HER-4蛋白在正常結(jié)直腸組織中未見(jiàn)陽(yáng)性表達(dá),而在結(jié)直腸癌病灶中呈現(xiàn)高表達(dá),且與淋巴結(jié)轉(zhuǎn)移、TNM分期密切相關(guān),高表達(dá)者預(yù)示著病程較晚,預(yù)后較差。HER-4不僅是一個(gè)有價(jià)值的生物標(biāo)志物,而且是一個(gè)潛在的抗癌治療靶點(diǎn)。

      [參考文獻(xiàn)]

      [1] Center MM,Jemal A,Ward E. International trends in colorectal cancer incidence rates[J]. Cancer Epidemiol Biomarkers Prev,2009,18(6):1688-1694.

      [2] Ferlay J,Steliarova-Foucher E,Lortet-Tieulent J,et al. Cancer incidence and mortality patterns in Europe:Estimates for 40 countries in 2012[J]. Eur J Cancer,2013,49(6):1374-1403.

      [3] Siegel R,Desantis C,Jemal A. Colorectal cancer statistics, 2014[J]. CA Cancer J Clin,2014,64(2):104-117.

      [4] Sun J,Jiang T,Qiu Z,et al. Short-term and medium-term clinical outcomes of laparoscopic-assisted and open surgery for colorectal cancer:A single center retrospective case-control study[J]. BMC Gastroenterol,2011,11(1):85.

      [5] Biondi A,Grosso G,Mistretta A,et al. Laparoscopic-Assisted versus open surgery for colorectal cancer:Short and long-term outcomes comparison[J]. J Laparoendosc Adv Surg Tech A,2013,23(1):1-7.

      [6] Jayne DG,Thorpe HC,Copeland J,et al. Five-year follow-up of the Medical Research Council CLASICC trial of laparoscopically assisted versus open surgery for colorectal cancer[J]. Br J Surg,2010,97(11):1638-1645.

      [7] Tebbutt N,Pedersen MW,Johns TG. Targeting the ERBB family in cancer:Couples therapy[J]. Nat Rev Cancer,2013, 13(9):663-673.

      [8] Montemurro F,Scaltriti M. Biomarkers of drugs targeting HER-family signalling in cancer[J]. J Pathol,2014,232(2):219-229.

      [9] Pinto AC,Ades F,de Azambuja E,et al. Trastuzumab for patients with HER2 positive breast cancer:Delivery,duration and combination therapies[J]. Breast,2013,22(Suppl 2):S152-S155.

      [10] Yan M,Parker BA,Schwab R,et al. HER2 aberrations in cancer:implications for therapy[J]. Cancer Treat Rev,2014, 40(6):770-780.

      [11] Sithanandam G,Anderson LM. The ERBB3 receptor in cancer and cancer gene therapy[J]. Cancer Gene Ther,2008,15(7):413-448.

      [12] Lee CM,Shrieve DC,Zempolich KA,et al. Correlation between human epidermal growth factor receptor family(EGFR,HER2,HER3,HER4),phosphorylated Akt(P-Akt),and clinical outcomes after radiation therapy in carcinoma of the cervix[J]. Gynecol Oncol,2005,99(2):415-421.

      [13] Xia W,Lau YK,Zhang HZ,et al. Combination of EGFR, HER-2/neu,and HER-3 is a stronger predictor for the outcome of oral squamous cell carcinoma than any individual family members[J]. Clin Cancer Res,1999,5(12):4164-4174.

      [14] Lai C,Lemke G. An extended family of protein-tyrosine kinase genes differentially expressed in the vertebrate nervous system[J]. Neuron,1991,6(5):691-704.

      [15] Plowman GD,Culouscou JM,Whitney GS,et al. Ligand-specific activation of HER4/p180erbB4,a fourth member of the epidermal growth factor receptor family[J]. Proc Natl Acad Sci USA,1993,90(5):1746-1750.

      [16] Ljuslinder I,Malmer B,Isaksson-Mettavainio M,et al. ErbB 1-4 expression alterations in primary colorectal cancers and their corresponding metastases[J]. Anticancer Res,2009,29(5):1489-1494.

      [17] Zhao WY,Zhuang C,Xu J,et al. HER4 is a novel prognostic biomarker in gastrointestinal stromal tumor specifically originated from stomach[J]. Am J Cancer Res,2014, 4(6):838-849.

      [18] Kountourakis P,Pavlakis K,Psyrri A,et al. Prognostic significance of HER3 and HER4 protein expression in colorectal adenocarcinomas[J]. BMC Cancer,2006,6:46.

      [19] Lee JC,Wang ST,Chow NH,et al. Investigation of the prognostic value of coexpressed erbB family members for the survival of colorectal cancer patients after curative surgery[J]. Eur J Cancer,2002,38(8):1065-1071.

      [20] Baiocchi G,Lopes A,Coudry RA,et al. ErbB family immunohistochemical expression in colorectal cancer patients with higher risk of recurrence after radical surgery[J].Int J Colorectal Dis,2009,24(9):1059-1068.

      [21] He XX,Ding L,Lin Y,et al. Protein expression of HER2, 3,4 in gastric cancer:Correlation with clinical features and survival[J]. J Clin Pathol,2015,68(5):374-380.

      [22] Sasaki H,Okuda K,Kawano O,et al. ErbB4 expression and mutation in Japanese patients with lung cancer[J]. Clin Lung Cancer,2007,8(7):429-433.

      [23] Hollmen M,Maatta JA,Bald L,et al. Suppression of breast cancer cell growth by a monoclonal antibody targeting cleavable ErbB4 isoforms[J]. Oncogene,2009,28(10):1309-1319.

      (收稿日期:2016-08-02)

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