Hi,

We are trying to establish subcutaneous tumor in NSG mice using prostate cancer cell line PC3 (engineered with firefly luc). We use IVIS to monitor tumor growth and noticed that the tumor size (Fluc intensity) was largest on Day3, decreased half on Day7, and slowly increased in the following 2-3 weeks, but still not reaching or surpassing the reading on Day3. We worked with subcutaneous tumor model in NSG mice before using other cell lines (eg, lymphoma) and we have always observed very fast and exponential tumor growth.

So I would like to ask;

1. Is what we observed with PC3 cells normal?

2. Would other prostate cancer cell lines (Lncap, Du154) form better subcutaneous tumors in NSG mice?

3. Are there other ways to improve PC3 tumor growth in vivo? (We noticed that the PC3 tumors grow better with matrigel, but we would like to avoid matrigel usage if possible. Also there is this paper where they seemed to grow PC3 tumors just fine without matrigel:Article Combinatorial antigen recognition with balanced signaling pr...

Thank you!

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