Molecular pathological study on tumorigenesis of beta-catenin gene alterated foci in rat colon mucosa

大鼠结肠黏膜β-catenin基因改变灶致瘤的分子病理学研究

基本信息

  • 批准号:
    13670208
  • 负责人:
  • 金额:
    $ 2.11万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    2001
  • 资助国家:
    日本
  • 起止时间:
    2001 至 2003
  • 项目状态:
    已结题

项目摘要

Although beta-catenin accumulated crypts(BCAC)is an useful biomarker in the retrieval of the chemopreventive agents on rat colon carcinogenesis, the detection of BCAC is complicated, since the preparation manufacture is needed.In this study, it was examined the mucin or mucoprotein in neoplastic lesions using the High-iron diamine alcian blue(HID+AB) PH2.5 and AB pH1.0 staining for dissolving these problems.Negative lesions by the HID+AB pH2.5 staining were significantly included in BCAC, further than the aberrant crypt foci(ACE), that is conventional lesions in rat colon carcinogenesis.Especially, the rate of concordance between negative lesion nest HID+AB pH2.5 staining and BCAC which consist of crypts over 4 was high.Therefore, the negative lesion, which consisted of crypts over 4, was able to seem to become the substitution of BCAC.However, the detection of BCAC in the proximal colon was difficult for the HID+AB pH2.5 staining because of the characteristics of the histological feature of proximal colon and the HLD+AB pH2.5 staining. Thus, we examined the possibility of the application of AB pH1.0 alone staining by which sulfomucin and sialomucin can be simultaneously represented as well as HJD+AB pH2.5 staining.The AB pH1.0 alone staining was able to detect the negative lesions easier than HID+AB pH2.5 staining, and it was also proven that the detection was possible on those in the proximal colon.In conclusion, both HID+AB pH2.5 staining and AB pH1.0 alone staining were detectable the conventional preneoplastic lesions such as BCAC and ACF.In the future, it is necessary to search the mutual relationship among these negative lesions, BCAC and ACF.
β -连环蛋白积累隐窝(-catenin accumulation crypts, BCAC)是一种有用的生物标志物,可用于大鼠结肠癌化学预防药物的检测,但由于BCAC的制备需要,其检测过程较为复杂。本研究采用高铁二胺阿利新蓝(HID+AB) PH2.5和AB pH1.0染色法检测肿瘤病变中的粘蛋白或粘蛋白,以解决这些问题。在BCAC中,HID+AB pH2.5染色阴性的病变比大鼠结肠癌的常规病变异常隐窝灶(ACE)更明显。特别是,阴性病变巢HID+AB pH2.5染色与由4个以上隐窝组成的BCAC的一致性率很高。因此,由超过4个隐窝组成的阴性病变似乎能够成为BCAC的替代品。然而,由于近端结肠的组织学特征和HLD+AB pH2.5染色的特点,HID+AB pH2.5染色较难检测近端结肠的BCAC。因此,我们研究了AB pH1.0单独染色的可能性,该染色可以同时表示磺胺和唾液蛋白,以及HJD+AB pH2.5染色。AB pH1.0单独染色比HID+AB pH2.5染色更容易检测到阴性病变,并且也证明了对近端结肠的检测是可能的。综上所述,HID+AB pH2.5染色和AB pH1.0单独染色均可检测到BCAC、ACF等常规瘤前病变。今后需要进一步研究这些阴性病变与BCAC、ACF之间的相互关系。

项目成果

期刊论文数量(18)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Kanamori T, Itoh M, Yoshimi N: "Pressure dye-spray : a simple and reliable method for differeintiating adenomas from hyperplastic polyps in the colon"Gastrointest.Endosc.. 55. 695-700 (2002)
Kanamori T、Itoh M、Yoshimi N:“压力染料喷雾:一种简单可靠的区分结肠腺瘤和增生性息肉的方法”Gastrointest.Endosc.. 55. 695-700 (2002)
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    0
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Shimizu, M., Yoshimi, N.et al.: "No involvement of β-catenin gene mutation in gastric carcinomas induced by N-methyl-N-nitrosourea in male F344 rats."Cancer Letter. 195. 147-152 (2003)
Shimizu, M., Yoshimi, N.等人:“雄性 F344 大鼠中 N-甲基-N-亚硝基脲诱导的胃癌与 β-连环蛋白基因突变无关。”Cancer Letter. 195. 147-152 (2003) )
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Yoshimi N, Matsunaga K, et al.: "The inhibitory effects of mangiferin, a naturally occurring glucosylxanthone, in bowel carcinogenesis of male F344 rats."Cancer Lett.. 163・2. 163-170 (2001)
Yoshimi N、Matsunaga K 等人:“芒果苷(一种天然存在的葡萄糖基黄酮)对雄性 F344 大鼠肠癌发生的抑制作用。”Cancer Lett.. 163・2 (2001)。
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    0
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Yamada Y, Yoshimi N, et al.: "Sequential analysis of morphological and biological properties of β-catenin-accumulated crypts, provable premalignant lesions independent of aberrant crypt foci in rat colon carcinogenesis"Cancer Res.. 61. 1874-1878 (2001)
Yamada Y、Yoshimi N 等人:“β-连环蛋白累积隐窝的形态学和生物学特性的序列分析,可证明的癌前病变独立于大鼠结肠癌发生中的异常隐窝病灶”Cancer Res.. 61. 1874-1878 (2001 )
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    0
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Matsunaga K, Yoshimi N et al.: "Inhibitory effects of chlorogenic acid on azoxymethane-induced colon carcinogenesis in male F344 rats"Asian Pacific J Cancer Prev.. 3(2). 163-166 (2002)
Matsunaga K、Yoshimi N 等人:“绿原酸对雄性 F344 大鼠氧化偶氮甲烷诱导的结肠癌的抑制作用”Asian Pacific J Cancer Prev.. 3(2)。
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YOSHIMI Naoki其他文献

YOSHIMI Naoki的其他文献

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{{ truncateString('YOSHIMI Naoki', 18)}}的其他基金

Morphological and molecular pathological study of mucin -depleted foci as the preneoplastic lesion for depressed flat type on colon carcinogenesis
粘蛋白缺失病灶作为凹陷扁平型结肠癌癌前病变的形态学和分子病理学研究
  • 批准号:
    20590405
  • 财政年份:
    2008
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
β-catenin gene mutations in rat inflammation-induced colon carcinogenesis model and the modification and influence on histopathological and morphological change of the neoplastic lesions
炎症诱导的大鼠结肠癌模型中β-catenin基因突变及其对肿瘤病变组织病理形态学变化的修饰及影响
  • 批准号:
    11670210
  • 财政年份:
    1999
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
The enzyme expressions of arachidonic acid cascade in rat colon carcinogenesis and modifying effects of chemopreventive agents
花生四烯酸级联酶在大鼠结肠癌发生中的表达及化学预防药物的调节作用
  • 批准号:
    07670237
  • 财政年份:
    1995
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

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