Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Abstract 1708: Heparanase regulates response to chemotherapy in myeloma

View through CrossRef
Abstract Following therapy, essentially all multiple myeloma patients relapse due to a population of chemoresistant cells leading to eventual patient death. Our lab has identified heparanase, an endoglycosidase, as a master regulator of aggressive myeloma disease. In the present study that was designed to probe the role of heparanase in chemoresistance, we made the striking finding that heparanase promotes survival of tumor cells post-therapy. Using an array of cellular viability assays, we tested for differences in viability and apoptosis between myeloma cells engineered to express high levels of heparanase (HPSE-high) and cells expressing low levels of heparanase (HPSE-low) following their exposure to frontline anti-myeloma drugs (bortezomib, carfilzomib). Results revealed a much smaller apoptotic fraction and higher cell viability following treatment of the HPSE-high cells compared to HPSE-low cells. In addition to promoting tumor survival, we also discovered that myeloma cell expression and secretion of heparanase is dramatically enhanced in response to chemotherapy. Using small molecule inhibitors, we were able to pinpoint that activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) was driving the heparanase expression upon chemotherapy. The secreted heparanase generated by chemotherapy was readily taken up by tumor cells growing in culture, consistent with previous studies demonstrating that heparanase is taken up by myeloma tumor cells and that this activates aggressive tumor behavior. Extending our findings to the clinic revealed that in tumor cells from seven out of nine myeloma patients examined, there was a dramatic increase in heparanase gene expression following chemotherapy. Together, these results demonstrate a pivotal role for heparanase in regulating myeloma response to therapy and indicate that the use of heparanase inhibitors may inhibit or delay relapse in myeloma. Citation Format: Vishnu Prakash C. Ramani, Fenghuang Zhan, Guido Tricot, Ralph D. Sanderson. Heparanase regulates response to chemotherapy in myeloma. [abstract]. In: Proceedings of the 105th Annual Meeting of the American Association for Cancer Research; 2014 Apr 5-9; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2014;74(19 Suppl):Abstract nr 1708. doi:10.1158/1538-7445.AM2014-1708
Title: Abstract 1708: Heparanase regulates response to chemotherapy in myeloma
Description:
Abstract Following therapy, essentially all multiple myeloma patients relapse due to a population of chemoresistant cells leading to eventual patient death.
Our lab has identified heparanase, an endoglycosidase, as a master regulator of aggressive myeloma disease.
In the present study that was designed to probe the role of heparanase in chemoresistance, we made the striking finding that heparanase promotes survival of tumor cells post-therapy.
Using an array of cellular viability assays, we tested for differences in viability and apoptosis between myeloma cells engineered to express high levels of heparanase (HPSE-high) and cells expressing low levels of heparanase (HPSE-low) following their exposure to frontline anti-myeloma drugs (bortezomib, carfilzomib).
Results revealed a much smaller apoptotic fraction and higher cell viability following treatment of the HPSE-high cells compared to HPSE-low cells.
In addition to promoting tumor survival, we also discovered that myeloma cell expression and secretion of heparanase is dramatically enhanced in response to chemotherapy.
Using small molecule inhibitors, we were able to pinpoint that activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) was driving the heparanase expression upon chemotherapy.
The secreted heparanase generated by chemotherapy was readily taken up by tumor cells growing in culture, consistent with previous studies demonstrating that heparanase is taken up by myeloma tumor cells and that this activates aggressive tumor behavior.
Extending our findings to the clinic revealed that in tumor cells from seven out of nine myeloma patients examined, there was a dramatic increase in heparanase gene expression following chemotherapy.
Together, these results demonstrate a pivotal role for heparanase in regulating myeloma response to therapy and indicate that the use of heparanase inhibitors may inhibit or delay relapse in myeloma.
Citation Format: Vishnu Prakash C.
Ramani, Fenghuang Zhan, Guido Tricot, Ralph D.
Sanderson.
Heparanase regulates response to chemotherapy in myeloma.
[abstract].
In: Proceedings of the 105th Annual Meeting of the American Association for Cancer Research; 2014 Apr 5-9; San Diego, CA.
Philadelphia (PA): AACR; Cancer Res 2014;74(19 Suppl):Abstract nr 1708.
doi:10.
1158/1538-7445.
AM2014-1708.

Related Results

Microwave Ablation with or Without Chemotherapy in Management of Non-Small Cell Lung Cancer: A Systematic Review
Microwave Ablation with or Without Chemotherapy in Management of Non-Small Cell Lung Cancer: A Systematic Review
Abstract Introduction  Microwave ablation (MWA) has emerged as a minimally invasive treatment for patients with inoperable non-small cell lung cancer (NSCLC). However, whether it i...
Heparanase and Survivin—potential markers of aggressiveness of colon cancers
Heparanase and Survivin—potential markers of aggressiveness of colon cancers
14524 Background: Survivin is an inhibitor of apoptosis and specifically expressed in several human cancers. Heparanase seems to play an important role in cancer metastasis, angio...
Data from Functional B7.2 and B7-H2 Molecules on Myeloma Cells Are Associated with a Growth Advantage
Data from Functional B7.2 and B7-H2 Molecules on Myeloma Cells Are Associated with a Growth Advantage
<div>Abstract<p><b>Purpose:</b> B7 family molecules expressed on antigen-presenting cells stimulate or inhibit normal immune responses. The aim of this stud...
Data from Functional B7.2 and B7-H2 Molecules on Myeloma Cells Are Associated with a Growth Advantage
Data from Functional B7.2 and B7-H2 Molecules on Myeloma Cells Are Associated with a Growth Advantage
<div>Abstract<p><b>Purpose:</b> B7 family molecules expressed on antigen-presenting cells stimulate or inhibit normal immune responses. The aim of this stud...
MAF Protein Elicits Innate Resistance To Bortezomib In Multiple Myeloma
MAF Protein Elicits Innate Resistance To Bortezomib In Multiple Myeloma
Abstract Multiple myeloma (MM) is a malignancy of terminally differentiated clonal plasma cells displaying significant molecular heterogeneity with 7 subgroups defin...
Plasma Cell Disorders
Plasma Cell Disorders
Multiple myeloma represents 1.4% of all new patients with cancer and will result in an estimated 11,090 deaths in 2014. It is twice as common in black men as in white men and 2.5 t...
Plasma Cell Disorders
Plasma Cell Disorders
Multiple myeloma represents 1.4% of all new patients with cancer and will result in an estimated 11,090 deaths in 2014. It is twice as common in black men as in white men and 2.5 t...
Focal MIBI uptake is a better indicator of active myeloma than diffuse uptake
Focal MIBI uptake is a better indicator of active myeloma than diffuse uptake
Abstract:  Purpose: Technetium‐99m 2‐methoxyisobutylisonitrile (MIBI) imaging has been proposed as a front‐line investigation to detect bone disease both before and after the trea...

Back to Top