Cancers 2014, 6(1), 42-66; doi:10.3390/cancers6010042

The Complex Function of Hsp70 in Metastatic Cancer

Center for Advanced Bioanalysis GmbH, Gruberstr. 40-42, A-4020 Linz, Austria
* Author to whom correspondence should be addressed.
Received: 7 November 2013; in revised form: 5 December 2013 / Accepted: 11 December 2013 / Published: 20 December 2013
(This article belongs to the Special Issue Heat Shock Proteins in Cancer: Chaperones of Tumorigenesis)
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Abstract: Elevated expression of the inducible heat shock protein 70 (Hsp70) is known to correlate with poor prognosis in many cancers. Hsp70 confers survival advantage as well as resistance to chemotherapeutic agents, and promotes tumor cell invasion. At the same time, tumor-derived extracellular Hsp70 has been recognized as a “chaperokine”, activating antitumor immunity. In this review we discuss localization dependent functions of Hsp70 in the context of invasive cancer. Understanding the molecular principles of metastasis formation steps, as well as interactions of the tumor cells with the microenvironment and the immune system is essential for fighting metastatic cancer. Although Hsp70 has been implicated in different steps of the metastatic process, the exact mechanisms of its action remain to be explored. Known and potential functions of Hsp70 in controlling or modulating of invasion and metastasis are discussed.
Keywords: Hsp70; metastasis; invasion; trafficking; lysosome

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MDPI and ACS Style

Juhasz, K.; Lipp, A.-M.; Nimmervoll, B.; Sonnleitner, A.; Hesse, J.; Haselgruebler, T.; Balogi, Z. The Complex Function of Hsp70 in Metastatic Cancer. Cancers 2014, 6, 42-66.

AMA Style

Juhasz K, Lipp A-M, Nimmervoll B, Sonnleitner A, Hesse J, Haselgruebler T, Balogi Z. The Complex Function of Hsp70 in Metastatic Cancer. Cancers. 2014; 6(1):42-66.

Chicago/Turabian Style

Juhasz, Kata; Lipp, Anna-Maria; Nimmervoll, Benedikt; Sonnleitner, Alois; Hesse, Jan; Haselgruebler, Thomas; Balogi, Zsolt. 2014. "The Complex Function of Hsp70 in Metastatic Cancer." Cancers 6, no. 1: 42-66.

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