Article citationsMore>>
Bettegowda, C., Sausen, M., Leary, R.J., Kinde, I., Wang, Y., Agrawal, N., Bartlett, B.R., Wang, H., Luber, B., Alani, R.M., Antonarakis, E.S., Azad, N.S., Bardelli, A., Brem, H., Cameron, J.L., Lee, C.C., Fecher, L.A., Gallia, G.L., Gibbs, P., Le, D., Giuntoli, R.L., Goggins, M., Hogarty, M.D., Holdhoff, M., Hong, S.M., Jiao, Y., Juhl, H.H., Kim, J.J., Siravegna, G., Laheru, D.A., Lauricella, C., Lim, M., Lipson, E.J., Marie, S.K., Netto, G.J., Oliner, K.S., Olivi, A., Olsson, L., Riggins, G.J., Sartore-Bianchi, A., Schmidt, K., Shih, L., Oba-Shinjo, S.M., Siena, S., Theodorescu, D., Tie, J., Harkins, T.T., Veronese, S., Wang, T.L., Weingart, J.D., Wolfgang, C.L., Wood, L.D., Xing, D., Hruban, R.H., Wu, J., Allen, P.J., Schmidt, C.M., Choti, M.A., Velculescu, V.E., Kinzler, K.W., Vogelstein, B., Papadopoulos, N. and Diaz, L.A. (2014) Detection of Circulating Tumor DNA in Early- and Late-Stage Human Malignancies. Science Translational Medicine, 6, 224ra24.
https://doi.org/10.1126/scitranslmed.3007094
has been cited by the following article:
-
TITLE:
Detection of the PIK3CA Mutation in Circulating Tumor DNA as a Possible Predictive Indicator for Poor Prognosis of Early-Stage Breast Cancer
AUTHORS:
Ayaka Sato, Masahiko Tanabe, Yumi Tsuboi, Masako Ikemura, Keiichiro Tada, Yasuyuki Seto, Yoshinori Murakami
KEYWORDS:
Early-Stage Breast Cancer, PIK3CA, Circulating Tumor DNA, Plasma, Droplet Digital PCR
JOURNAL NAME:
Journal of Cancer Therapy,
Vol.9 No.1,
January
26,
2018
ABSTRACT: Objectives: Circulating tumor DNA (ctDNA) is shown to provide the real-time genomic information of metastatic breast cancer. This
study elucidates the clinico-pathological significance of ctDNA in early-stage breast
cancer using the PIK3CA mutation as an indicator. Materials and Methods: Twenty-seven primary breast cancers without metastasis were surgically resected and pathologically diagnosed at the University of Tokyo Hospital, Japan. Genomic
DNA of primary tumor was extracted from formalin-fixed and paraffin-embedded
specimens. ctDNA was extracted from fresh-frozen plasma from patients. The PIK3CA mutations at E542K, E545K and H1047R were
examined by Sanger sequencing or droplet digital PCR in 27 tumors and
pre- and post-surgery plasma. Results: The PIK3CA mutations were detected in
13 (48%) of 27 primary tumors. These mutations did not significantly correlate
with specific clinico-pathological characteristics of tumors. When ctDNA was
examined, 4 (33%) of 12 cases carrying the mutated PIK3CA showed the
identical mutation in pre-surgery plasma and 2 (50%) of them showed the identical
mutations in post-surgery plasma. Interestingly, in these 2 cases in
pathological stages IIIA and IA, fractional abundance of the mutated PIK3CA alleles to the total alleles in pre-surgery ctDNA was around 1% or more
and was higher than that of the other two cases without PIK3CA mutations in
post-surgery ctDNA. Conclusions: The PIK3CA mutation in ctDNA is detectable even
in a subset of early-stage breast cancer. Furthermore, fractional abundance of
the mutated PIK3CA in pre-surgery ctDNA could provide a possible predictive
indicator for tumor burden and for choosing the appropriate adjuvant treatment
of breast cancer.
Related Articles:
-
Minzhi Wei, Yujian Gan, Shengqiang Tang
-
Jai Dev Chandel, Nand Lal Singh
-
Ananda Prasad Panta, Ram Prasad Ghimire, Dinesh Panthi, Shankar Raj Pant
-
Du Thanh Hang, Than Thi Thanh Tra, Le Minh Tuan, Geoffrey Peter Savage
-
Casimir Komenan