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体内恶性乳腺肿瘤内钴胺素摄取的影像学研究。

Imaging Cobalamin Uptake within Malignant Breast Tumors In Vivo.

机构信息

Department of Radiology, Mayo Clinic, Rochester, MN, USA.

出版信息

Mol Imaging Biol. 2019 Apr;21(2):356-367. doi: 10.1007/s11307-018-1232-9.

Abstract

PURPOSE

To image the uptake of cobalamin (Cbl) within malignant breast tumors in vivo.

PROCEDURES

Prior to surgery 20 female patients with clinically suspected breast tumors were intravenously administered 0.25 μg of an In-111 labeled 5-deoxyadenosylcobalamin (AC) analog ([In]AC) and sequentially imaged with whole-body planar (WBP) and single-photon emission computed tomography (SPECT) between 2-5 h and 20-24 h post-injection (P.I.). The tumor to background (T/B) ratio for [In]AC in breast tumors at 2-5 h was correlated to its expression of estrogen (ER), progesterone (PR), and human epidermal growth factor 2 (HER2) receptors. Subsequent pulse chase (PC) experiments in nude mice burdened with the MDA-MB-231 triple-negative (TN) breast tumor xenograft measured the effect that pulses of AC or dexamethasone (DEX) had on [In]AC uptake in both normal murine tissue and the TN breast tumor.

RESULTS

The mean [In]AC T/B ratio of the patients' 18 resected tumors was 5.8. Comparing ER- and PR-positive tumors (n = 11) to TN and HER2-positive tumors (n = 7), the mean [In]AC T/B ratios at 2-5 h P.I. were 3.2 (range 1.8-5.6) and 10.4 (range 3.3-22.5), respectively. Pulses of 2.0 μg of AC at 2, 8, or 24 h; or 40.0 μg of DEX at 24 h prior to injecting 0.5 μg of [In]AC, increased mean tracer uptake in the MDA-MB-231 tumors by 26.4, 71.5, 92.6, and 49.1 %, respectively. Only the 2- and 24-h PC intervals concomitantly suppressed [In]AC uptake in normal murine tissue while enhancing [In]AC uptake in MDA-MB-231 tumors.

CONCLUSION

The uptake of Cbl within malignant breast tumors can be imaged clinically. Cbl uptake is greatest in TN and HER2-positive breast tumors. A solitary bolus of AC or DEX increases the [In]AC uptake within a breast tumor in vivo. Investigating the cytogenetic mechanisms controlling the endocytosis of Cbl in malignant breast tumors is warranted.

摘要

目的

在体内对恶性乳腺肿瘤的钴胺素(Cbl)摄取进行成像。

过程

在手术前,20 名临床怀疑患有乳腺肿瘤的女性患者静脉注射 0.25μg 的放射性核素标记的 5-脱氧腺苷钴胺素(AC)类似物([In]AC),并在注射后 2-5 小时和 20-24 小时之间进行全身平面(WBP)和单光子发射计算机断层扫描(SPECT)连续成像(P.I.)。在乳腺肿瘤中,[In]AC 在 2-5 小时的肿瘤与背景(T/B)比值与雌激素(ER)、孕激素(PR)和人表皮生长因子 2(HER2)受体的表达相关。随后在携带 MDA-MB-231 三阴性(TN)乳腺癌异种移植的裸鼠中进行脉冲追踪(PC)实验,测量 AC 或地塞米松(DEX)脉冲对正常鼠组织和 TN 乳腺癌中[In]AC 摄取的影响。

结果

18 例切除肿瘤患者的平均[In]AC T/B 比值为 5.8。将 ER 和 PR 阳性肿瘤(n=11)与 TN 和 HER2 阳性肿瘤(n=7)进行比较,注射后 2-5 小时的平均[In]AC T/B 比值分别为 3.2(范围 1.8-5.6)和 10.4(范围 3.3-22.5)。在注射 0.5μg [In]AC 之前,在 2、8 或 24 小时给予 2.0μg 的 AC 脉冲,或在 24 小时给予 40.0μg 的 DEX,可使 MDA-MB-231 肿瘤的平均示踪剂摄取分别增加 26.4%、71.5%、92.6%和 49.1%。只有 2 小时和 24 小时的 PC 间隔同时抑制了正常鼠组织中[In]AC 的摄取,同时增强了 MDA-MB-231 肿瘤中[In]AC 的摄取。

结论

恶性乳腺肿瘤内 Cbl 的摄取可以在临床上进行成像。在 TN 和 HER2 阳性的乳腺癌中,Cbl 的摄取量最大。单次给予 AC 或 DEX 可增加体内乳腺癌肿瘤中的[In]AC 摄取。值得研究控制恶性乳腺癌肿瘤内 Cbl 内吞的细胞遗传学机制。

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