CRIPTO1 is a member of the family of proteins of the epidermal growth factor-CRIPTO1 / FRL1 / Cryptic (EGF-CFC) that performs specific functions during embryonic development and tumor. In the first case, it acts as required co-receptor for Nodal in the correct establishment of embryonic axys. In the second case, it was found that it is secreted at high levels by a variety of human cancers (colon, breast, lung, testis, ovary, pancreas and stomach etc.), but is absent or is weakly expressed in normal tissues. Therefore, this study was to ascertain the presence of CR1 in healthy placenta and those with invasiveness disorders, since the development of trophoblast in maternal fetal interface resembles in many ways the oncogenic process. Our results showed a pattern of distinct expression between first and third trimester of pregnancy, with the presence of CR3 and CR1, respectively. Choriocarcinoma were also immunoreactive for the protein, which still showed a positive relationship with the placenta acreta. Our in vitro studies have shown that recombinant CR1 has inducing action in HTR8/SV-Neo cells, significantly increasing the invasion and migration, the latter process is significantly abolished in the presence of RNA interference. In conclusion, CRIPTO1 is expressed mainly in extravillous cytotrophoblast cells in normal pregnancy in the first and third trimester of pregnancy. In the first trimester the distribution of this expression in the process of differentiation in cells in invasive cells suggests a role in this process. In placenta acreta with the increased of the trophoblastic invasiveness besides the endometrial limits, there is an increased expression of this factor, which is also found in malignant choriocarcinoma cytotrophoblast cells. The immunolocalization of CRIPTO1 in these samples strongly suggests the involvement of this factor in functional activities of trophoblast cells, such as invasiveness and differentiation. The increase in migration of these cells after treatment with CRIPTO1 and the attenuation of this process in cells with CRIPTO gene silenced confirm experimentally the action of this protein in the trophoblastic cells. This study contributes to the identification of factors associated with trophoblast invasiveness in normal and pathological conditions.