[HTML][HTML] Search for KPNA7 cargo proteins in human cells reveals MVP and ZNF414 as novel regulators of cancer cell growth

EM Vuorinen, NK Rajala, HE Rauhala… - … et Biophysica Acta (BBA …, 2017 - Elsevier
EM Vuorinen, NK Rajala, HE Rauhala, AT Nurminen, VP Hytönen, A Kallioniemi
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, 2017Elsevier
Abstract Karyopherin alpha 7 (KPNA7) belongs to a family of nuclear import proteins that
recognize and bind nuclear localization signals (NLSs) in proteins to be transported to the
nucleus. Previously we found that KPNA7 is overexpressed in a subset of pancreatic cancer
cell lines and acts as a critical regulator of growth in these cells. This characteristic of KPNA7
is likely to be mediated by its cargo proteins that are still mainly unknown. Here, we used
protein affinity chromatography in Hs700T and MIA PaCa-2 pancreatic cancer cell lines and …
Abstract
Karyopherin alpha 7 (KPNA7) belongs to a family of nuclear import proteins that recognize and bind nuclear localization signals (NLSs) in proteins to be transported to the nucleus. Previously we found that KPNA7 is overexpressed in a subset of pancreatic cancer cell lines and acts as a critical regulator of growth in these cells. This characteristic of KPNA7 is likely to be mediated by its cargo proteins that are still mainly unknown. Here, we used protein affinity chromatography in Hs700T and MIA PaCa-2 pancreatic cancer cell lines and identified 377 putative KPNA7 cargo proteins, most of which were known or predicted to localize to the nucleus. The interaction was confirmed for two of the candidates, MVP and ZNF414, using co-immunoprecipitation, and their transport to the nucleus was hindered by siRNA based KPNA7 silencing. Most importantly, silencing of MVP and ZNF414 resulted in marked reduction in Hs700T cell growth. In conclusion, these data uncover two previously unknown human KPNA7 cargo proteins with distinct roles as novel regulators of pancreatic cancer cell growth, thus deepening our understanding on the contribution of nuclear transport in cancer pathogenesis.
Elsevier