淺論金屬硫蛋白過表達(dá)對乳腺癌化療方案選擇的影響

1、淺論金屬硫蛋白過表達(dá)對乳腺癌化療方案選擇的影響                  作者：董建峰 馬潔華 張輝 張曉麗 薄愛華【摘要】  目的：探討金屬硫蛋白(Metallothionein，MT)在乳腺癌中過表達(dá)的意義及其與乳腺癌化療方案選擇的相關(guān)性。方法：利用SP免疫組織化學(xué)技術(shù)，檢測88例乳腺癌組織中MT表達(dá)率。結(jié)果：MT在乳腺癌中總陽性率為67.05%(59/88)。MT在髓樣癌、小葉癌和導(dǎo)管癌中的陽性率分別為41.67

2、%，85.71%和62.50%。在浸潤型乳腺癌組陽性率明顯高于非浸潤型癌組(P0.05);在小葉癌組陽性率高于髓樣癌組和導(dǎo)管癌組(P0.05);淋巴結(jié)轉(zhuǎn)移組陽性率高于非轉(zhuǎn)移組(P0.05)。結(jié)論：MT表達(dá)與乳腺癌的病理類型及有否淋巴結(jié)轉(zhuǎn)移相關(guān)，檢測MT對乳腺癌化療方案的制定有指導(dǎo)意義。 【關(guān)鍵詞】  金屬硫蛋白;乳腺腫瘤;免疫組織化學(xué)Since the first report of metallothionein(MT)overexpression in thyroid cancer tissues by Cherian and Nartey in 19871,there has

3、been an extensive interest in the role which is played by MT in tumorigenesis.The abnormal increase of MT is related to the genesis,development and drugresistance of tumor.To investigate the expression of MT in breast cancer and its clinical significance,we collected 88 cases with breast cancer to e

4、xamine the expression of MT with streptavidin peroxidase(SP)immunohistochemical method,The aim was to clarify the relation between the expression of MT and the biology characteristic of tumor cell,and offer a base of establishing chemistry treatment scheme.1 Materials and methods1.1 Patients and sam

5、ples88 cases with breast cancer in women were collected from January 2005 to October 2008 at No.1 Affiliated Hospital Hebei North University in Zhangjiakou.The age range was 30 to 79 years old,the average age was 51.5 years,and the median age was 48.5 years.1.2 Immunohistochemical stainingMouse anti

6、metallothionein antibody was conducted by Santa Cruz,USA.Immunohistochemical staining SP kit and DAB kit were purchased from Beijing Zhongshan Goldenbridge biotechnology Co.Ltd.(China).The samples of cancer were fixed in 100mL/L dehydrated formaldehyde and embedded in paraffin,sections of 5m thickne

7、ss were sliced,which were dyed by HE staining method,and all samples were confirmed by pathological diagnosis and clinical classitication.Immunohistochemical SP staining method was used in the experiment with conventional staining procedures.The negative control was designed as PBS instead of antibo

8、dy I,the positive control was known as positive tissue sections which was provided by Beijing Zhongshan Co.Ltd.(China).1.3 Statistical analysis2 test was used for statistical analysis,P value less than 0.05 was considered as statistical significance.2 ResultsThe MT immunoreactive productions was sho

9、wed brown with yellow color and distributed in cytoplasm of the cancer cells.But the cell nucleus and negative control cell were showed no color(Fig13).The relationship between the expression of MT and the biology characteristic of carcinomer cell was showed in Tables 1.Table 1 Relationship between

10、MT expression and pathology type,lymph metastases in breast cancerGroupnBreast Cancer MT(+)n%Total positive rate885967.05Marrow cancer12541.67Lobular cancer282485.71Ductal carcinoma483062.50Infiltrating cancer 685276.47Noninfiltrating cancer20735.00Lymph metastases393076.92Nonlymph metastases492959.

11、18:Positive rate was significantly higher than that of marrow cancer group and ductal carcinoma group(P0.05);:Positive rate was significantly higher than that of noninfiltrating cancer group(P0.05);:Positive rate was significantly higher than that of Nonlymph metastases group(P0.05)Fig 1 Infiltratin

12、g ductal carcinoma (SP,×400)Fig 2 Infiltrating lobular cancer (SP,×400)Fig 3 Marrow cancer (SP,×400) DiscussionThe MT is protein of small molecular with much sulfydryl.MT gene is located at chromosome 16.MT proteins are small molecular weight proteins containing 61 to 68 amino acid re

13、sidue,and are characterized by high cysteine content with a paucity of aromatic acids,there is 25%30% cysteine of in MT.In human,there are four subgroup of MT proteins,namely MT1,MT2,MT3 and MT4,and each subgroup can be classified into and .Because MT exhibit the selective chelating power for heavy

14、metal ion such as zine(Zn),copper(Cu),cadmium(Cd)and platinum(Pt),they are involved in heavy metal complex.MT has close relation to absorption，transportation and metabolism of many trace elements.MT has also been implicated in chemoresistance to anticancer drugs and in scavenging free radical in cel

15、ls.The clearance ability of MT is 38.5 times higher than that of glutathione according to the relevant report,especially ZnMT.Moreover,MT also participates in the regulation of stress reaction and cell apoptosis.Some reports indicated that the high expression of MT had some relation to the occurrenc

16、e,development and differentiation of tumor.         MT gene is inducible,its involvement in tumor drugresistance has attracted much attention,Huang Gengwen et altransfected C127 cells of mouse with human MT gene,resulting in 10 times more MT content along with

17、 4.4 times increase of drugresistance to carboplatin, chlorambucil and melpalan.Examined MT of many tumor cell lines,it was found that high expression of MT in cells was accompanied by drugresistance to cisplatin and alkylating agent,while cells with low expression of MT was sensitive to the above a

18、nticancer drugs.CdCl2 induced inhibition of MT gene expression in mouse embryonic fibrocytes could increase the sensitivity to anticancer drugs.The tumors with high MT expression have drugresistance to electrophilic chemotherapy drugs,it can cut off the effect of the chemotherapy drugs to targeted D

19、NA.When MT meets alkylating agent,it can change on property and structure,then affect the distribution of metal ion in cells,and start multiple chemical reactions,so that the cytotoxicity effect of alkylating agent is reduced.Some experiments demonstrated that tumors with high MT content were resist

20、ant to alkylating agents(carboplatin,cisplatin and nitrosocarbamidealkylating agent)and cyclophosphamide,but responsive to fluorouracil(5Fu)and vincristine.The mechanism needs further investigation.10,11.This study showed that positive rate of MT was higher in breast carcinoma,the total expression r

21、ate of MT was 67.05%,and the positive rate of MT in lobular cancer was higher than that of ductal cancer and marrow cancer(P0.05).The positive rat of MT was significantly higher in infiltrating type of cancer group than that in noninfiltrating type of cancer.The overexpression of MT showed was assoc

22、iated with biology characteristic of breast carcinoma.It was reported that the medicine of platinum(oxaliplatin,cisplatin etc.)is used widely in treating cancer at present,if the patients MT expression is high,his sensitivity will descend with this medicine,but to the patient with MT negative,his se

23、nsitivity will increase12,13.Our experiment indicated that it will enhance chemotherapy effect if drugresistance gene protein examination could be used broadly,it will enhance the rate of existence and the quantity of the patientslife.【參考文獻(xiàn)】  1 Shukla VK,Aryya NC,Pitale A,et al.Metallothionein expression in carcinoma of the gallbladderJ.Histopathology,1998,33:1541572 Jin R,Bay BH,Chow VT,et