Division of Cancer Prevention Research, National Cancer Center Research Institute, 5-1-1 Chuo-ku, Tokyo, 104-0045, Japan.
Ann Nucl Med. 2013 Aug;27(7):640-7. doi: 10.1007/s12149-013-0729-1. Epub 2013 Apr 23.
Lung cancer is one of the leading causes of cancer-related deaths worldwide, including Japan. Although computed tomography (CT) can detect small lung lesions such as those appearing as ground glass opacity, it cannot differentiate between malignant and non-malignant lesions. Previously, we have shown that single photon emission computed tomography (SPECT) imaging using (111)In-1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetic acid-cyclo-(Arg-Gly-Asp-D-Phe-Lys) (DOTA-c(RGDfK)), an imaging probe of αvβ3 integrin, is useful for the early detection of pancreatic cancer in a hamster pancreatic carcinogenesis model. In this study, we aimed to assess the usefulness of SPECT/CT with (111)In-DOTA-c(RGDfK) for the evaluation of the malignancy of lung cancer.
Lung tumors were induced by a single intraperitoneal injection (250 mg/kg) of urethane in male A/J mice. Twenty-six weeks after the urethane treatment, SPECT was performed an hour after injection of (111)In-DOTA-c(RGDfK). Following this, the radioactivity ratios of tumor to normal lung tissue were measured by autoradiography (ARG) in the excised lung samples. We also examined the expression of αvβ3 integrin in mouse and human lung samples.
Urethane treatment induced 5 hyperplasias, 41 adenomas and 12 adenocarcinomas in the lungs of 8 A/J mice. SPECT with (111)In-DOTA-c(RGDfK) could clearly visualize lung nodules, though we failed to detect small lung nodules like adenoma and hyperplasias (adenocarcinoma: 66.7%, adenoma: 33.6%, hyperplasia: 0.0%). ARG analysis revealed significant uptake of (111)In-DOTA-c(RGDfK) in all the lesions. Moreover, tumor to normal lung tissue ratios increased along with the progression of carcinogenesis. Histopathological examination using human lung tissue samples revealed clear up-regulation of αvβ3 integrin in well-differentiated adenocarcinoma (Noguchi type B and C) rather than atypical adenomatous hyperplasia.
Although there are some limitations in evaluating the malignancy of small lung tumors using (111)In-DOTA-c(RGDfK), SPECT with (111)In-DOTA-c(RGDfK) might be a useful non-invasive imaging approach for evaluating the characteristics of lung tumors in mice, thus showing potential for use in humans.
肺癌是全球癌症相关死亡的主要原因之一,包括在日本。虽然计算机断层扫描(CT)可以检测到肺部的小病变,如磨玻璃密度影,但它无法区分良恶性病变。此前,我们已经表明,使用(111)In-1,4,7,10-四氮杂环十二烷-N,N',N'',N'''-四乙酸-环-(Arg-Gly-Asp-D-Phe-Lys)(DOTA-c(RGDfK))作为 αvβ3 整联蛋白的成像探针的单光子发射计算机断层扫描(SPECT)成像对于在仓鼠胰腺癌变模型中早期检测胰腺癌是有用的。在这项研究中,我们旨在评估 SPECT/CT 与(111)In-DOTA-c(RGDfK)在评估肺癌恶性程度方面的用途。
雄性 A/J 小鼠经腹腔内单次注射(250mg/kg)尿烷诱导肺癌。在尿烷处理后 26 周,注射(111)In-DOTA-c(RGDfK)后 1 小时进行 SPECT。之后,通过切除肺样本中的放射性自显影(ARG)测量肿瘤与正常肺组织的放射性比值。我们还检查了小鼠和人肺样本中 αvβ3 整联蛋白的表达。
尿烷处理在 8 只 A/J 小鼠的肺部诱导了 5 个增生、41 个腺瘤和 12 个腺癌。(111)In-DOTA-c(RGDfK)的 SPECT 可以清楚地显示肺结节,但我们未能检测到像腺瘤和增生这样的小肺结节(腺癌:66.7%,腺瘤:33.6%,增生:0.0%)。ARG 分析显示所有病变均有明显的(111)In-DOTA-c(RGDfK)摄取。此外,随着癌变的进展,肿瘤与正常肺组织的比值增加。使用人肺组织样本的组织病理学检查显示,在分化良好的腺癌(Noguchi 型 B 和 C)中,αvβ3 整联蛋白明显上调,而不是非典型腺瘤性增生。
尽管使用(111)In-DOTA-c(RGDfK)评估小肺癌的恶性程度存在一些局限性,但(111)In-DOTA-c(RGDfK)的 SPECT 可能是一种有用的非侵入性成像方法,可用于评估小鼠肺部肿瘤的特征,因此在人类中具有应用潜力。