Possible association between Taenia solium cysticercosis and cancer: increased frequency of DMA damage in peripheral lymphocytes from neurocysticercosis patients
La. Herrera et al., Possible association between Taenia solium cysticercosis and cancer: increased frequency of DMA damage in peripheral lymphocytes from neurocysticercosis patients, T RS TROP M, 94(1), 2000, pp. 61-65
Citations number
27
Categorie Soggetti
Medical Research General Topics
Journal title
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE
Helminths, particularly some Schistosoma species, have been associated with
cancer in humans. Neurocysticercosis produced by cysticerci of the helmint
h Taenia solium, has been associated with the emergence of brain tumours an
d haematological malignancies. Local tumours, such as glioblastoma, could b
e explained by the induction of DNA damage in cells surrounding the cystice
rcus and chronically exposed to an inflammatory host response. However, sys
temic effects such as haematological malignancies are not easy to understan
d. The present work was conducted in Mexico: to find out whether DNA damage
arises in peripheral lymphocytes in patients with neurocysticercosis. We u
tilized a highly sensitive technique to analyse chromosomal aberrations, in
-situ hybridization with probes against chromosomes 1, 2 and 4, and in addi
tion the blocked-cytokinesis technique was used to determine the formation
of micronuclei, a peculiar form of DNA damage. The study was made in lympho
cytes from 8 patients before and after the administration of praziquantel,
1 of the 2 drugs used for neurocysticercosis treatment. The frequencies of
chromosome aberrations and micronuclei in peripheral blood lymphocytes were
higher in the infected patients as compared to those observed both in heal
thy donors and in the group of patients after praziquantel therapy. Our res
ults suggest that chromosome aberrations induced in peripheral cells during
neurocysticercosis could be associated with the development of haematologi
cal neoplasias.