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. 2012 Aug 2;104(16):1228–1239. doi: 10.1093/jnci/djs321

Table 1.

Alterations in plasma proteins in response to phenethyl isothiocyanate (PEITC) treatment in mouse mammary tumor virus (MMTV)-neu mice

Protein name Master No. Protein ID Ratio of protein abundance,
 PEITC vs control* P
α-Fetoprotein‡ 168 1 1.55 .07
Transferrin (Mus musculus) 275 2 1.49 .05
α-2-Macroglobulin‡ 1159 19 1.47 .05
α-Fetoprotein‡ 1045 20 1.97 .03
Chain L, crystal structure of the Fab fragment of mouse
    anti-human Fas antibody Hfe7a 1335 21 1.65 .05
α-2-Macroglobulin‡ 1248 22 2.01 .01
Chain L, Fab fragment of neutralizing monoclonal antibody
    4c4 complexed with G-H loop from Fmdv‡ 1333 23 2.63 .06
Apoa1 protein (Mus musculus) 1380 24 1.88 .05
Anti-human seminoprotein monoclonal antibody (Mus
    musculus) 1390 25 2.14 .05
Chain L, Fab fragment of neutralizing monoclonal antibody
    4c4 complexed with G-H loop from Fmdv‡ 1306 26 1.63 .02
α-Fetoprotein‡ 1125 28 –2.96 .05
Transthyretin (Mus musculus) 1181 29 7.10 .02
Chain L, human immunodeficiency virus-1 capsid protein
    (P24) complex with Fab25.3 1382 34 1.53 .01
Immunoglobulin light chain variable region (Mus musculus) 1354 36 2.05 .01
Predicted hypothetical protein (Mus musculus) 1953 38 –1.54 .02
Novel member of the major urinary protein gene family
    (Mus musculus) 1742 40 –3.52 .04
Albumin (Mus musculus) 1711 41 –1.49 .04

* Plasma samples used were from MMTV-neu mice fed either control diet or 3 µmol PEITC/g diet (n = 3 mice per group). They were separated by two-dimensional electrophoresis and compared.

† All P values were calculated by two-sided Student’s t tests.

‡ The protein spots likely represent isoforms or posttranslational modification(s) of the same protein.