| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Regular Articles |
Pharmaceutical Sciences Research Institute, Aston University, Birmingham, United Kingdom
 |
ABSTRACT |
|---|
 Top ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
- and ß-subunits and subunit p42 of the 19S regulator. The primary event in PIF-induced protein degradation is thought to be release of arachidonic acid from membrane phospholipids, and this process was attenuated by EPA, but not HMB, suggesting that HMB might act at another step in the PIF signaling pathway. EPA and HMB at a concentration of 50 µmol/L attenuated PIF-induced activation of protein kinase C and the subsequent degradation of inhibitor 
B and nuclear accumulation of nuclear factor B. EPA and HMB also attenuated phosphorylation of p42/44 mitogen-activated protein kinase by PIF, thought to be important in PIF-induced proteasome expression. These results suggest that HMB attenuates PIF-induced activation and increased gene expression of the ubiquitin-proteasome proteolytic pathway, reducing protein degradation. |
INTRODUCTION |
|---|
|
TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
In a previous report,1
we have shown protein degradation in skeletal muscle of mice bearing the MAC16 cachexia-inducing tumor to be attenuated by ß-hydroxy-ß-methylbutyrate (HMB) by inhibition of the increased expression of the ubiquitin-proteasome pathway. Although some cytokines, such as tumor necrosis factor (TNF-), have been shown to induce expression of the ubiquitin-proteasome pathway in skeletal muscle (4)
, there is no evidence for cytokine involvement in the MAC16 cachexia model (5)
. Instead, a tumor product, proteolysis-inducing factor (PIF), appears to be responsible for the loss of muscle mass (6)
, also through induction of key regulatory elements for proteasome proteolysis (7)
. PIF expression has been found in carcinomas of the prostate (8)
, colon, lung, esophagus, liver, and pancreas when weight loss is apparent (9)
but not in normal prostate tissue or stromal cells. It previously has been shown that the action of PIF is attenuated by the polyunsaturated fatty acid eicosapentaenoic acid (EPA; ref. 10
), which suppresses protein degradation in skeletal muscle through inhibition of the increased expression of the ubiquitin-proteasome proteolytic pathway (11)
. The action of EPA is manifested by interference with the PIF signaling pathway in muscle cells, leading to increased proteasome expression.
The full details of this pathway still have to be elucidated, but the first step involves the release of arachidonic acid from membrane phospholipids and the rapid metabolism to a range of eicosanoids, of which 15-hydroxyeicosatetraenoic acid (15-HETE) alone is capable of inducing protein degradation (10)
, by increasing proteasome expression (12)
. EPA attenuates the release of arachidonic acid and its metabolism to 15-HETE (10)
. Induction of proteasome expression by PIF (13)
and 15-HETE (12)
also was associated with an increased nuclear accumulation of the transcription factor nuclear factor B (NFB) and transitory depletion of inhibitor B (IB) from the cytosol, a process also attenuated by EPA. This process requires protein kinase C (PKC), which probably is involved in the phosphorylation and degradation of IB, necessary for the release of NFB from its inactive cytosolic complex (14)
.
This study examines the effect of HMB on PIF-induced protein degradation and signaling pathways in murine myotubes, in comparison with EPA, to determine the mechanism of the attenuation of the increased expression of the ubiquitin-proteasome proteolytic pathway observed in a murine model of cancer-induced weight loss.
|
MATERIALS AND METHODS |
|---|
|
TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
1, 2, 3, 5, 6, and 7 (clone MCP231), 20S proteasome subunit ß3 (HC10), and 19S regulator ATPase subunit Rpt 4 (S106, p42; clone p42–23) were purchased from BIOMOL International (Plymouth Meeting, PA). Rabbit polyclonal antisera to murine IB, phospholipase A2 (PLA2), type V1, and PKC were from Calbiochem (La Jolla, CA). Mitogen-activated protein kinase (MAPK) and the phosphorylated (active) forms were detected with anti–extracellular signal-regulated kinase (ERK) 1 and 2 [pTpY185/187] nonphospho-specific and phospho-specific rabbit polyclonal antisera (Biosource International, Camarillo, CA). Rabbit polyclonal antisera to mouse actin were from Sigma-Aldridge. Peroxidase-conjugated goat antirabbit and rabbit antimouse secondary antibodies were from Dako (Carpinteria, CA). Hybond nitrocellulose membranes and enhanced chemiluminescence were from Amersham Biosciences. Electrophoretic mobility shift (EMSA) gel shift assay kits were from Panomics (Redwood City, CA). Fetal calf serum, horse serum (HS), and Dulbecco’s modified Eagle’s medium (DMEM) were purchased from Life Technologies, Inc. (Rockville, MD).
Cell Culture.
C2C12 myotubes were routinely passaged in DMEM supplemented with 10% fetal calf serum, glutamine, and 1% penicillin-streptomycin under an atmosphere of 10% CO2 in air at 37°C. Myotubes were formed by allowing confluent cultures to differentiate in DMEM containing 2% HS, with medium changes every 2 days.
Purification of Proteolysis-Inducing Factor.
PIF was purified from solid MAC16 tumors (15)
excised from mice with a weight loss of 20 to 25%. Tumors were homogenized in 10 mmol/L Tris-HCl (pH 8.0) containing 0.5 mmol/L phenylmethylsulfonyl fluoride, 0.5 mmol/L EGTA, and 1 mmol/L dithiothreitol at a concentration of 5 mL/g tumor. Solid ammonium sulfate was added to 40% w/v, and the supernatant, after removal of the ammonium sulfate, was subjected to affinity chromatography using anti-PIF monoclonal antibody coupled to a solid matrix as described previously (16)
. The immunogenic fractions were concentrated and used for further studies.
Measurement of Total Protein Degradation.
Myotubes in six-well multidishes were labeled with L-[2,6–3H]phenylalanine (0.67 mCi/mmol) for 24 hours in 2 mL DMEM containing 2% HS. They then were washed three times in PBS, followed by a 2-hour incubation at 37°C in DMEM without phenol red until no more radioactivity appeared in the supernatant. Cells then were preincubated for 2 hours with and without EPA or HMB and then for 24 hours with PIF in fresh DMEM without phenol red to prevent quenching of counts and in the presence of 2 mmol/L cold phenylalanine to prevent reincorporation of radioactivity. The amount of radioactivity released into the medium was expressed as a percentage of control cultures not exposed to PIF.
Measurement of Arachidonate Release.
Myotubes in six-well multidishes containing 2 mL DMEM with 2% HS were labeled for 24 hours with 10 µmol/L arachidonic acid (containing 1 µCi [3H]arachidonate/mL; ref. 10
). Cells then were washed extensively with PBS to remove traces of unincorporated [3H]arachidonate, and either EPA or HMB was added 2 hours before PIF. After an additional 24 hours, 1 mL of medium was removed to determine the radioactivity released.
Measurement of Proteasome Activity.
The functional activity of the ß-subunits of the proteasome was determined as the "chymotrypsin-like" enzyme activity determined fluorimetrically according to the method of Orino et al. (17)
. Myotubes were exposed to PIF for 24 hours with or without EPA or HMB added 2 hours before PIF, and enzyme activity was determined in a supernatant fraction (13)
by the release of aminomethyl coumarin (AMC) from succinyl-LLVY-AMC (0.1 mmol/L) in the presence or absence of the specific proteasome inhibitor lactacystin (10 µmol/L; ref. 18
). Only lactacystin-suppressible activity was considered to be proteasome specific. Activity was adjusted for the protein concentration of the sample determined using the Bradford assay (Sigma Chemical Co., St. Louis, MO) using bovine serum albumin as standard.
Western Blot Analysis.
Cytosolic protein (2 to 5 µg) obtained for the aforementioned assay was resolved on 10% SDS-PAGE and transferred to 0.45 µm nitrocellulose membrane, which had been blocked with 5% Marvel in PBS, at 4°C overnight. The primary antibodies were used at a dilution of 1:100 (antiactin), 1:500 (anti-ERK1/2, PKC, and PLA2), 1:1000 (anti-20S proteasome ß-subunit and IB), 1:1500 (anti-20S proteasome -subunit), or 1:5000 (anti-p42), whereas the secondary antibodies were used at a dilution of 1:2000. Incubation was carried out for 2 hours at room temperature, and development was by enhanced chemiluminescence. Loading was quantitated by actin concentration.
Electrophoretic Mobility Shift.
DNA binding proteins were extracted from myotubes by the method of Andrews and Faller (19)
, which uses hypotonic lysis followed by high salt extraction of nuclei. The EMSA binding assay was carried out according to the manufacturer’s instructions.
Statistical Analysis.
Differences in means between groups were determined by one-way ANOVA, followed by Tukey-Kramer multiple comparison test.
|
RESULTS |
|---|
|
TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
. The effect of HMB has been compared with EPA, and the data in Fig. 1A
show that at a concentration of 50 µmol/L both were equally effective in attenuating PIF-induced protein degradation. There also was some attenuation at 25 µmol/L HMB at low, but not at high, concentrations of PIF, which appeared to potentiate the effect of PIF alone.
|
, as was protein degradation (Fig. 1A)
. The effect of PIF was completely attenuated by 50 µmol/L EPA and 25 and 50 µmol/L HMB, although 25 µmol/L HMB produced an increase in "chymotrypsin-like" enzyme activity at 10 nmol/L PIF as observed with protein degradation (Fig. 1A)
. A similar effect was observed on expression of proteasome 20S -subunits, ß-subunits, and p42, an ATPase subunit of the 19S regulator that promotes ATP-dependent association of the 20S proteasome with the 19S regulator to form the 26S proteasome (ref. 20
; Fig. 2
). In all of the cases, expression was increased by PIF at 4.2 and 10 nmol/L, and this was attenuated by EPA and HMB at 50 µmol/L but not at 25 µmol/L. These results confirm that HMB attenuates protein degradation through an effect on PIF induction of the ubiquitin-proteasome pathway.
|
, but HMB at 50 µmol/L had no effect on this process, suggesting that it acts farther down the pathway. At 25 µmol/L, HMB caused a significant increase in release of AA when combined with 10 nmol/L PIF, suggesting a mechanism for the increased protein degradation (Fig. 1A)
and chymotrypsin-like enzyme activity (Fig. 1B)
and proteasome expression (Fig. 2)
at this concentration. PIF caused an up-regulation of calcium-independent cytosolic PLA2 at 4.2 and 10 nmol/L (Fig. 4)
, corresponding with the maximal effect on AA release (Fig. 3)
. This effect was attenuated by EPA, but not HMB, at both concentrations. This suggests that HMB attenuates PIF-induced proteasome expression at a step in the intracellular signaling pathway after PLA2. Experiments using mutants of PKC and inhibitors of this enzyme show that this forms a central mediator of intracellular signaling by PIF (14)
. PIF stimulates translocation of PKC from the cytoplasm to the plasma membrane (Fig. 5)
, resulting in activation, with a maximum effect at 4.2 nmol/L PIF, as with protein degradation (Fig. 1)
. This process was effectively attenuated by EPA and HMB at 50 µmol/L, whereas HMB was less effective at 25 µmol/L (Fig. 5)
. This suggests that HMB attenuates PIF-induced protein degradation through inhibition of PKC.
|
|
|
. There was no effect on total ERK1/2 (Fig. 6A)
, whereas PIF induced an increased phosphorylation of p42/44, which was maximal at 4.2 nmol/L, and this effect was completely attenuated by EPA and HMB at 50 µmol/L but not by HMB at 25 µmol/L (Fig. 6B)
. The ability of HMB to attenuate ERK1/2 phosphorylation suggests that this step is after the activation of PKC and also may be important in inhibition of PIF-induced proteasome expression by HMB.
|
B and stimulates nuclear accumulation of NFB, and this process has been shown to be attenuated by 50 µmol/L EPA (13)
. The results in Fig. 7A
show HMB at 50 µmol/L to effectively attenuate IB degradation in the presence of PIF in murine myotubes and to prevent nuclear accumulation of NFB (Fig. 7D)
. Only partial inhibition of binding of NFB to DNA was observed when HMB was used at a concentration of 25 µmol/L (Fig. 7C)
. These results suggest that the overall effect of HMB is similar to that of EPA in preventing movement of NFB into the nucleus with concomitant activation of gene expression.
|
|
DISCUSSION |
|---|
|
TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
In many respects the effect of HMB is similar to that of EPA, which also attenuates the increased proteasome proteolysis in cancer-induced weight loss (11)
. Both are equipotent, and both inhibit PIF-induced signaling pathways. PIF previously has been reported to induce activation of PLA2 (22)
, with release of arachidonic acid from membrane phospholipids, as a primary event in the signaling cascade. EPA has been shown to block the release of AA and the conversion to 15-HETE (10)
, whereas HMB has no effect on this process. Low concentrations (25 µmol/L) of HMB combined with higher concentrations of PIF (10 nmol/L) appear to increase release of AA, which may account for the stimulation of protein breakdown and expression of the ubiquitin-proteasome pathway at these concentrations. PIF induced protein degradation with a parabolic dose-response curve as reported previously (10
, 12
, 13)
. The shape of the dose-response curve is thought to result from the requirement of PKC in the signaling pathway (14)
. Overstimulation of PKC results in down-regulation of activity. The first step at which HMB inhibits PIF signaling appears to be through PKC. EPA also appears to block PKC, but this may be an indirect effect because AA and lipoxygenase metabolites have been shown to activate PKC (28)
. PIF also has been shown to activate phospholipase C (PLC), and this step also is involved in the increase in proteasome expression (22)
. Activation of phospholipase C would result in the generation of diacylglycerol, which also could induce translocation of PKC from the cytosol to the plasma membrane, resulting in the complete activation of the kinase. PKC appears to be important in the induction of proteasome expression by PIF because it was blocked by inhibitors of PKC and in myotubes transfected with a dominant-negative PKC, which showed no activation of PKC (14)
. Thus, the ability of HMB to block activation of PKC by PIF would explain the ability to inhibit proteasome expression and the subsequent increase in protein degradation. The mechanism of the inhibitory effect of HMB is not known; it may be direct or may be caused by inhibition of phospholipase C.
Activation of PKC may induce phosphorylation and activation of the IB kinase complex (29)
responsible for the phosphorylation of IB at serine-32 and -36, leading to ubiquitination and subsequent degradation by the proteasome system. Degradation of IB releases NFB, which then is able to enter the nucleus and stimulate gene expression by binding to its target elements. Induction of proteasome expression by PIF (13)
and 15-HETE (12)
appears to require NFB because the NFB inhibitor peptide SN50 also attenuated the increase in proteasome expression. Myotubes transfected with mutants at the serine phosphorylation sites of IB, which are required for degradation, also were resistant to PIF-induced protein degradation and proteasome expression.2
If HMB attenuates PIF-induced activation of PKC, then downstream signaling pathways, namely, degradation of IB and nuclear accumulation of NFB, also would be inhibited, as was observed, thus explaining the ability of HMB to attenuate the PIF-induced increase in the ubiquitin-proteasome pathway.
The ERK/MAPK pathway also was shown to be important in PIF-induced proteasome expression (22)
. Thus, PIF induces phosphorylation of ERK1 and ERK2 at the same concentrations as those inducing proteasome expression, whereas a selective inhibitor of MAP/ERK kinase attenuated the PIF-induced activation of ERK1 and ERK2 and the induction of proteasome expression. The ERK/MAPK pathway is an intracellular transduction system mainly involved in the cellular response to growth factors and is activated through tyrosine kinase receptors, acting through small G proteins, such as Ras (30)
. It previously has been shown (20)
that two tyrosine kinase inhibitors, genistein and tryptostin A23, attenuated the PIF-induced increase in proteasome activity, suggesting the involvement of tyrosine kinase in this process. The PKC pathway is linked to the MAPK pathway through multiple steps. Thus, stimulation of G-protein receptors can indirectly activate MAPK through the PKC pathway (31)
. It has been proposed that PKC phosphorylates and activates Raf-1 kinase, a substrate not only for the isoforms but also for the other PKC isozymes, ß and 
(32)
, and this in turn leads to activation of MAPK through the kinase cascade (33)
. The MAPK pathway may provide an alternative mechanism for proteasome expression in addition to NFB.
Thus, HMB appears to be an effective agent for the management of muscle wasting in cancer-induced weight loss. HMB appears to exert its effect by attenuation of PIF-induced protein degradation mediated through the ubiquitin-proteasome pathway by inhibition of PKC, with resultant stabilization of the cytoplasmic IB/NFB complex.
|
FOOTNOTES |
|---|
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
Requests for reprints: Michael J. Tisdale, Pharmaceutical Sciences Research Institute, Aston University, Birmingham, B4 7ET, United Kingdom.
1 Smith HJ, Mukerji P, Tisdale MJ. Attenuation of proteasome-induced proteolysis in skeletal muscle by ß-hydroxy-ß-methylbutyrate in cancer cachexia. Cancer Res. In press 2004. 
Received 5/19/04. Revised 8/19/04. Accepted 9/27/04.
|
REFERENCES |
|---|
|
TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
or interleukin-6. Cancer Lett 1992;65:239-43.[CrossRef][Medline]
B. Br J Cancer 2003;89:1116-22.[CrossRef][Medline]
B in proteolysis-inducing factor-induced proteasome expression in C2C12 myotubes. Br J Cancer 2004;90:1850-7.[Medline]
is an upstream activator of the IB kinase complex in the TPA signal transduction pathway to NF-B in U20S cells. Cell Sig 2000;12:759-68.[CrossRef][Medline]
activates Raf-1 by direct phosphorylation. Nature 1993;364:249-52.[CrossRef][Medline]This article has been cited by other articles:
|
|
 |
|
  M. J. Tisdale Mechanisms of Cancer Cachexia Physiol Rev, April 1, 2009; 89(2): 381 - 410. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S. Baier, D. Johannsen, N. Abumrad, J. A. Rathmacher, S. Nissen, and P. Flakoll Year-long Changes in Protein Metabolism in Elderly Men and Women Supplemented With a Nutrition Cocktail of {beta}-Hydroxy-{beta}-methylbutyrate (HMB), L-Arginine, and L-Lysine JPEN J Parenter Enteral Nutr, January 1, 2009; 33(1): 71 - 82. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 H. L. Eley, S. T. Russell, and M. J. Tisdale Mechanism of attenuation of muscle protein degradation induced by tumor necrosis factor-{alpha} and angiotensin II by {beta}-hydroxy-{beta}-methylbutyrate Am J Physiol Endocrinol Metab, December 1, 2008; 295(6): E1417 - E1426. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
H. L. Eley, S. T. Russell, J. H. Baxter, P. Mukerji, and M. J. Tisdale Signaling pathways initiated by beta-hydroxy-beta-methylbutyrate to attenuate the depression of protein synthesis in skeletal muscle in response to cachectic stimuli Am J Physiol Endocrinol Metab, October 1, 2007; 293(4): E923 - E931. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 M. F. McCarty and K. I. Block Toward a Core Nutraceutical Program for Cancer Management Integr Cancer Ther, June 1, 2006; 5(2): 150 - 171. [Abstract] [PDF]
|
|
|
|
 |
|
 R. Siddiqui, D. Pandya, K. Harvey, and G. P. Zaloga Nutrition Modulation of Cachexia/Proteolysis Nutr Clin Pract, April 1, 2006; 21(2): 155 - 167. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. J. Tisdale Clinical Anticachexia Treatments Nutr Clin Pract, April 1, 2006; 21(2): 168 - 174. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 V. E. Baracos and M. L. Mackenzie Investigations of Branched-Chain Amino Acids and Their Metabolites in Animal Models of Cancer J. Nutr., January 1, 2006; 136(1): 237S - 242S. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Cancer Research | Clinical Cancer Research |
| Cancer Epidemiology Biomarkers & Prevention | Molecular Cancer Therapeutics |
| Molecular Cancer Research | Cancer Prevention Research |
| Cancer Prevention Journals Portal | Cancer Reviews Online |
| Annual Meeting Education Book | Meeting Abstracts Online |
) or 25 µmol/L (
) or 50 µmol/L (
) HMB. Measurements were made 24 hours after the addition of PIF and are shown as mean ± SE, where n = 9. Differences from control in the absence of PIF are indicated as a (P < 0.005), whereas differences from PIF alone in the presence of EPA or HMB are shown as b (P < 0.01) and c (P < 0.005). B, chymotryptic activity of soluble extracts of murine myotubes treated with PIF in the absence or presence of EPA (50 µmol/L) or HMB (25 or 50 µmol/L). The symbols are the same as in A. The results are shown as mean ± SE, where n = 9. Differences from control are shown as a (P < 0.001), whereas differences in the presence of EPA or HMB are shown as b (P < 0.001).
), 50 µmol/L HMB (
