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. Author manuscript; available in PMC: 2015 Sep 1.
Published in final edited form as: Toxicol Appl Pharmacol. 2014 Jun 24;279(2):220–229. doi: 10.1016/j.taap.2014.06.010

Table 1.

Literature summary of in vivo tumor models where significant anti-tumor efficacy was reported when engineered PrAgs were administered in combination with various cytotoxins

Engineered PrAg Cytotoxin In vivo Tumor Model
MMP-activated PrAg, PrAg-L1 LF-HMAGGb LL3, Lewis lung carcinoma syngraft (22)
B16-BL6, melanoma syngraft (22)
C32, melanoma xenograft (22)
HT144, melanoma xenograft (22)
A549, lung carcinoma xenograft (22)
Colo205, colon carcinoma xenograft (22)
BHT-101, anaplastic thyroid carcinoma orthotopic implant (23)

uPA-activated PrAg, PrAg-U2 FP59c LL3, Lewis lung carcinoma syngraft (19,20)
T241, fibrosarcoma syngraft (19,20)
B16-BL6, melanoma syngraft (19,20)
HT1299, non-squamous cell lung carcinoma xenograft (21)

LFa B16-BL6, melanoma syngraft (25)

dual MMP/uPA-activated PrAg, IC-PrAg (PrAg-L1-I210A + PrAg-U2-R200A) FP59c LL3, Lewis lung carcinoma syngraft (8)
T241, fibrosarcoma syngraft (8)
B16-BL6, melanoma syngraft (8)

LF-HMAGGb HN12, head and neck squamous cell carcinoma xenograft (24)
HN6, head and neck squamous cell carcinoma (24)
Hep2, head and neck squamous cell carcinoma (24)
Cal27, head and neck squamous cell carcinoma (24)
a

LF is wild-type anthrax lethal factor, with the native N-terminal sequence AGG

b

LF-HMAGG is a version of LF having the non-native N-terminal sequence HMAGG

c

FP59 is a fusion protein containing the PrAg binding domain of LF fused to the catalytic domain of Pseudomonas aeruginosa exotoxin A