Identification of molecular basis for aggressive malignancies and drug resistance of renal cancer

Research Press Release | February 24, 2016

In clear cell renal cell carcinomas cells (ccRCCs), lysophosphatidic acid (LPA) activates Arf6 via its G-protein coupled receptors, in which GTP-bound Gα12 directly binds to the Arf6-specific guanine nucleotide exchanging factor, EFA6. Activated Arf6 then employs its downstream effector AMAP1, and AMAP1 then binds to the mesenchymal-specific protein EPB41L5, to promote invasion and metastasis, and drug resistance of ccRCCs. RhoA activity is dispensable to the mesenchymal malignancies induced by LPA.
In clear cell renal cell carcinomas cells (ccRCCs), lysophosphatidic acid (LPA) activates Arf6 via its G-protein coupled receptors, in which GTP-bound Gα12 directly binds to the Arf6-specific guanine nucleotide exchanging factor, EFA6. Activated Arf6 then employs its downstream effector AMAP1, and AMAP1 then binds to the mesenchymal-specific protein EPB41L5, to promote invasion and metastasis, and drug resistance of ccRCCs. RhoA activity is dispensable to the mesenchymal malignancies induced by LPA.


Key Points

・A major factor promoting malignancies of clear cell renal cell carcinomas (ccRCCs) is a lipid mediator, lysophosphatidic acid (LPA).


・LPA activates a small GTPase Arf6 and hence promotes mesenchymal malignancies and drug resistance.


・This Arf6 pathway includes a mesenchymal-specific protein that is not expressed in non-metastatic cancers.


・Blockade of the Arf6 pathway suppresses the mesenchymal malignancies and drug resistance.


・High levels of the mesenchymal-specific protein of this pathway provides a clear biomarker to identify treatable ccRCCs.

Outline

Clear cell renal cell carcinomas (ccRCCs) account for 70% to 80% of the kidney cancers. ccRCCs are often highly resistant to therapeutic drugs and ionizing radiation, and exhibit recurrence with a rate of 30-40% of the patients. Onset of the mesenchymal programs of ccRCCs has been highly implicated in their advanced malignancies, including invasiveness and high metastatic abilities. Scientists at Hokkaido University Graduate School of Medicine now reports that a lipid mediator lysophosphatidic acid (LPA) is the major factor that promotes mesenchymal malignancies of a large population of primary ccRCCs, together with fine molecular mechanisms therein involved.


LPA is well known to activate a small GTPase Rho, and has long been believed to thereby promote cancer malignancies. The research team led by Professor Hisataka Sabe have clarified that LPA activates another small GTPase, Arf6, in ccRCCs; and that Arf6 then needs a mesenchymal-specific protein EPB41L5, which is not normally expressed in epithelial cells, to promote invasion, metastasis and drug resistance. They have moreover demonstrated that RhoA activity is dispensable in these processes of the cancer malignancies. Analyses on pathology specimens reveal that high levels of expression of the Arf6-based pathway components, especially EPB41L5, exhibits statistical, tight correlations with poor overall survival of the patients. The kidneys are natural filers of body fluids, while, on the other hand, LPA can be produced easily in body fluids by an extracellular enzyme autotaxin. Thus, these results identified mechanisms as to how aggressive malignancies, as well as robust resistance to therapeutics, arise in many primary ccRCCs in response to a component of the body fluids. Since this research team has previously reported several methods that effectively causes blockade of Arf6 and its signaling pathway, these findings will provide excellent therapeutic opportunities toward many ccRCC patients.


Shigeru Hashimoto, a Specially Appointed Associate Professor of Hokkaido University, played a key role in this study. This study was performed in a collaboration with researchers of Keio University School of Medicine, Professor Mototsugu Oya and Senior Assistant Professor Shuji Mikami.

Inquiries

Hisataka SABE, Professor

Department of Molecular Biology, Hokkaido University Graduate School of Medicine

sabeh[at]med.hokudai.ac.jp

Japanese Link

腎明細胞癌の浸潤・転移性並びに薬剤耐性の分子基盤の解明 (02.09.2016)

Publications

Lysophosphatidic acid activates Arf6 to promote the mesenchymal malignancy of renal cancerNature Communications (02.08.2016)

LATEST NEWS

University News | December 13, 2017
Japan-Russia Youth Forum 2017 held at Hokkaido University
University News | December 01, 2017
HU Ambassador wins the 2017 Volvo Environmental Prize
University News | November 13, 2017
Dinner meeting with Indonesian alumni
Student Awards | November 10, 2017
Student Awards: Graduate School of Medicine
University News | November 10, 2017
The 4th Joint Working Group 2017 Indonesia-Japan

ARCHIVES

CONNECT WITH US

  • Facebook
  • Twitter
  • Instagram
  • YouTube
  • LinkedIn

BACK TO TOP