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结肠大体肿瘤计数、卡尺直径测量与肿瘤负荷计算

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Tumor-burden endpoint for the AOM/DSS colitis-associated cancer model: at the day-100 endpoint mice are euthanized by cervical dislocation, the entire colon is excised into 15 ml cold sterile PBS, flushed with 5-10 ml cold PBS through a 21 G needle, opened longitudinally and rinsed again; macroscopic tumors are counted one by one, each tumor's diameter is measured with a digital caliper, and tumor load per mouse is the summed size of all its tumors. Photographed colons are fixed in 10% formalin solution (Sigma-Aldrich HT-501128) for paraffin sections and histological grading. Applies to AOM/DSS models (predominantly C57BL/6 background) for comparing tumor number, size distribution and intervention effects; the adopted record reports 100% tumor take in its in-house C57BL/6-background wild-type mice at day 100.

Scope and method

Sample:终点(AOM/DSS 方案约第 100 天)分离并纵向剖开的小鼠全结肠

histopathology assay

Reagents and materials

Procedure

  1. Procedure

    Open the mice using sterile forceps and scissors to carefully remove the entire colon and place it in a 10 cm Petri dish with 15 ml cold sterile PBS, which should be enough to cover the entire colon.

  2. Procedure

    Carefully hold the distal part of the colon with the help of forceps and then flush to remove feces with 5-10 ml cold sterile PBS using a 21 G needle attached to a 5 ml syringe. After flushing the feces, put the cleaned colon in a new Petri dish.

  3. Procedure

    Carefully open the colon longitudinally and rinse again with cold PBS to remove remaining feces.

  4. Procedure

    For the AOM/DSS experiment, count the macroscopic tumors in the longitudinally open colon. In our in-house bred mice with mostly C57BL/6 background, tumor development is observed in 100% of the WT animals. Tumor size (average diameter) is measured using a digital caliper and tumor load per mouse is calculated by summing up the sizes of all the tumors in a given mouse. After counting tumor numbers and load, longitudinally opened colons can be photographed (Figure 1) before fixing them as ”swiss-rolls” in 10% formalin solution and then embedding in paraffin. H&E stained paraffin sections (Figure 2) should be analyzed for tumor grading and immune cells infiltration by an experience pathologist.

Quality control and readouts

计数与测量在纵向剖开并漂洗去除粪便后的全结肠上进行;肿瘤负荷按每只动物全部肿瘤尺寸求和计算;大体计数后同一结肠固定并制备石蜡切片用于组织学确认。

每只动物的大体肿瘤数目、各肿瘤直径(卡尺测量)与肿瘤负荷(该动物全部肿瘤尺寸之和),配套照片与组织学分级输入;用于组间成瘤负担比较。

References

  1. Gupta J, Nebreda AR. Induction of Colitis and Colitis-associated Colorectal Cancer (CAC). Bio-protocol 4(22): e1290 (2014). DOI: 10.21769/BioProtoc.1290

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