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正电子发射断层扫描成像肿瘤细胞死亡使用镥-89 标记的 APOMAB ® 顺铂化疗后肺癌和卵巢癌异种移植模型。

Positron Emission Tomographic Imaging of Tumor Cell Death Using Zirconium-89-Labeled APOMAB® Following Cisplatin Chemotherapy in Lung and Ovarian Cancer Xenograft Models.

机构信息

Translational Oncology Laboratory, Centre for Cancer Biology, SA Pathology and University of South Australia, Level 9 University of South Australia Health Innovation Building, North Terrace, Adelaide, 5000, Australia.

School of Medicine, University of Adelaide, Adelaide, SA, 5000, Australia.

出版信息

Mol Imaging Biol. 2021 Dec;23(6):914-928. doi: 10.1007/s11307-021-01620-1. Epub 2021 Jul 6.

DOI:10.1007/s11307-021-01620-1
PMID:34231102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8578059/
Abstract

PURPOSE

Early detection of tumor treatment responses represents an unmet clinical need with no approved noninvasive methods. DAB4, or its chimeric derivative, chDAB4 (APOMAB®) is an antibody that targets the Lupus associated antigen (La/SSB). La/SSB is over-expressed in malignancy and selectively targeted by chDAB4 in cancer cells dying from DNA-damaging treatment. Therefore, chDAB4 is a unique diagnostic tool that detects dead cancer cells and thus could distinguish between treatment responsive and nonresponsive patients.

PROCEDURES

In clinically relevant tumor models, mice bearing subcutaneous xenografts of human ovarian or lung cancer cell lines or intraperitoneal ovarian cancer xenografts were untreated or given chemotherapy followed 24h later by chDAB4 radiolabeled with [Zr]Zr. Tumor responses were monitored using bioluminescence imaging and caliper measurements. [Zr]Zr-chDAB4 uptake in tumor and normal tissues was measured using an Albira SI Positron-Emission Tomography (PET) imager and its biodistribution was measured using a Hidex gamma-counter.

RESULTS

Tumor uptake of [Zr]Zr-chDAB4 was detected in untreated mice, and uptake significantly increased in both human lung and ovarian tumors after chemotherapy, but not in normal tissues.

CONCLUSION

Given that tumors, rather than normal tissues, were targeted after chemotherapy, these results support the clinical development of chDAB4 as a radiodiagnostic imaging agent and as a potential predictive marker of treatment response.

摘要

目的

肿瘤治疗反应的早期检测是一种未满足的临床需求,目前尚无经过批准的非侵入性方法。DAB4 或其嵌合衍生物 chDAB4(APOMAB®)是一种针对狼疮相关抗原(La/SSB)的抗体。La/SSB 在恶性肿瘤中过度表达,并且在因 DNA 损伤治疗而死亡的癌细胞中被 chDAB4 选择性靶向。因此,chDAB4 是一种独特的诊断工具,可检测死亡的癌细胞,从而可以区分治疗有反应和无反应的患者。

方法

在临床相关的肿瘤模型中,未治疗或接受化疗的荷有人卵巢或肺癌细胞系皮下异种移植或腹腔内卵巢癌异种移植的小鼠,随后在 24 小时后用 [Zr]Zr 标记的 chDAB4 进行放射性标记。使用生物发光成像和卡尺测量监测肿瘤反应。使用 Albira SI 正电子发射断层扫描(PET)成像仪测量肿瘤和正常组织中 [Zr]Zr-chDAB4 的摄取,并使用 Hidex 伽马计数器测量其生物分布。

结果

在未治疗的小鼠中检测到 [Zr]Zr-chDAB4 在肿瘤中的摄取,并且在化疗后两种人肺和卵巢肿瘤中的摄取均显著增加,但在正常组织中没有。

结论

鉴于化疗后仅靶向肿瘤而不是正常组织,这些结果支持将 chDAB4 作为放射性诊断成像剂以及作为治疗反应潜在预测标志物的临床开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/fb114578fd37/11307_2021_1620_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/ecadc6dcf486/11307_2021_1620_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/8504b4fe7e50/11307_2021_1620_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/f6358aff2900/11307_2021_1620_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/8d737fe3424a/11307_2021_1620_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/fb114578fd37/11307_2021_1620_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/ecadc6dcf486/11307_2021_1620_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/8504b4fe7e50/11307_2021_1620_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/f6358aff2900/11307_2021_1620_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/8d737fe3424a/11307_2021_1620_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7c/8578059/fb114578fd37/11307_2021_1620_Fig5_HTML.jpg

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