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烟草烟雾对大鼠Dunning R3327前列腺腺癌肿瘤生长及辐射反应的影响

Effects of tobacco smoke on tumor growth and radiation response of dunning R3327 prostate adenocarcinoma in rats.

作者信息

Johansson S, Landström M, Bjermer L, Henriksson R

机构信息

Department of Oncology, University Hospital Umeå, Umeå, Sweden.

出版信息

Prostate. 2000 Mar 1;42(4):253-9. doi: 10.1002/(sici)1097-0045(20000301)42:4<253::aid-pros2>3.0.co;2-3.

Abstract

BACKGROUND

The influence of tobacco smoke has been investigated on the growth rate and histology of prostate cancer, both in untreated tumors and in those subjected to fractionated irradiation.

METHODS

Twenty-five rats were implanted bilaterally with Dunning R3327 tumor fragments at 10 weeks of age. Approximately 3 months later, they were randomly allocated to two groups, one of which was exposed to tobacco smoke for an hour each day, 5 days a week. Three weeks later the groups were further subdivided into two groups which acted as controls or were subjected to 5 daily doses of 6 Gy. The tumors were measured weekly to construct growth curves. At a fixed time, 9 weeks or 20 weeks later, the animals were sacrificed and the tumors were removed for histological evaluation of the tissue composition. Sections from each tumor were scored in a morphometric analysis of the fraction of the area of tumor that was occupied by (epithelial) tumor cells, by stroma, or by luminal spaces. In addition, the density of mast cells was assessed in adjacent sections stained with toluidine blue.

RESULTS

Smoking caused only minor changes in the growth rates of both the control and the irradiated tumors. At the cellular level, smoking caused a small but significant increase in the fraction of tumor cells relative to controls. Irradiation also caused a small but significant decrease in tumor cell fraction compared to controls, even after 20 weeks of regrowth. This difference was reduced in the smoking and irradiation group. The main difference observed was in the mast cell numbers. Smoking caused a 4-fold increase in mast-cell density. Irradiation caused an even greater increase (25-fold). The combination of smoking and irradiation resulted in an intermediate increase (10-fold).

CONCLUSIONS

Long-term smoke exposure can slightly alter the growth rate and morphology of Dunning R3327 rat prostatic adenocarcinoma, but our study does not show a negative effect on the outcome of radiation treatment of this tumor model. We have also demonstrated a highly elevated number of mast cells in the irradiated group, and have shown that smoke exposure significantly depressed the radiation-induced enhancement of the number of mast cells.

摘要

背景

已对烟草烟雾对前列腺癌生长速率和组织学的影响进行了研究,研究对象包括未经治疗的肿瘤以及接受分次照射的肿瘤。

方法

25只大鼠在10周龄时双侧植入邓宁R3327肿瘤碎片。大约3个月后,将它们随机分为两组,其中一组每周5天每天暴露于烟草烟雾中1小时。3周后,这些组进一步细分为两组,一组作为对照,另一组每天接受5次6 Gy的照射。每周测量肿瘤大小以构建生长曲线。在固定时间,9周或20周后,处死动物并取出肿瘤进行组织组成的组织学评估。在形态计量分析中,对每个肿瘤的切片进行评分,分析肿瘤区域中被(上皮)肿瘤细胞、基质或管腔空间占据的比例。此外,在经甲苯胺蓝染色的相邻切片中评估肥大细胞的密度。

结果

吸烟仅使对照肿瘤和照射后肿瘤的生长速率发生轻微变化。在细胞水平上,与对照相比,吸烟导致肿瘤细胞比例有小幅但显著的增加。与对照相比,即使在再生长20周后,照射也导致肿瘤细胞比例有小幅但显著的降低。在吸烟和照射组中,这种差异有所减小。观察到的主要差异在于肥大细胞数量。吸烟使肥大细胞密度增加了4倍。照射导致的增加更大(25倍)。吸烟和照射相结合导致中等程度的增加(10倍)。

结论

长期接触烟雾可轻微改变邓宁R3327大鼠前列腺腺癌的生长速率和形态,但我们的研究未显示对该肿瘤模型的放射治疗结果有负面影响。我们还证明照射组中肥大细胞数量大幅增加,并表明接触烟雾显著抑制了照射诱导的肥大细胞数量增加。

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