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Experimental Therapeutics |
Valentis Inc., Burlingame, California 94010
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ABSTRACT |
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 Top ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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INTRODUCTION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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Angiostatin and endostatin are fragments of larger proteins, and they are generated in the extracellular compartment by proteolytic digestion of plasminogen (3
, 8)
or collagen XVIII (4)
, respectively. Release of a protease, metalloelastase, from infiltrating macrophages can produce angiostatin in Lewis lung carcinoma (9)
, and a similar activation mechanism may exist for endostatin. The tumor suppressor activity of angiostatin specifically targets proliferating endothelial cells, thereby blocking angiogenesis (10)
. One mechanism by which angiostatin is thought to inhibit proliferation is the binding to the 
/
-subunits of ATP synthase (11)
. Angiostatin may also function by inducing apoptotic cell death (10)
or by down-regulating vascular endothelial growth factor expression (12)
. Resistance of tumors to treatment, a common problem with small-molecule anticancer drugs, did not develop with angiostatin (13)
. Thus, the selectivity of angiostatin for tumor-derived endothelial cells coupled with a lack of toxicity and resistance after prolonged administration (13)
makes this protein a potentially valuable therapeutic for patients with advanced cancers. However, human angiostatin is a short-lived protein in animal models (13)
. To achieve complete tumor remission, relatively large quantities of protein must be given for extended periods of time (12
, 13)
, and this may limit the clinical use of angiostatin. An alternative strategy to avoid the problem is the gene therapeutic use of vectors that encode secreted angiostatin. To test the potential of a plasmid-based gene delivery, we generated an expression vector encoding secretable human angiostatin protein containing the four kringle domains (14)
. It has been shown that kringle 4 of angiostatin is the most potent domain in suppressing endothelial cell migration, whereas kringles 1–3 contain the entire growth inhibitory activity (15)
. The activity of angiostatin transgenes has recently been tested in several tumor models (16, 17, 18)
. A four-kringle murine angiostatin cDNA expressed in either T241 fibrosarcoma, RT2 glioma, or U87 MG glioblastoma cells suppressed tumor growth in mice (16
, 17)
, and the delivery of a human three-kringle angiostatin cDNA with an adenovirus to s.c. C6 glioma and MDA-MB-231 xenografts inhibited tumor growth by blocking endothelial cell proliferation (18)
. We tested whether plasmid-based expression of a four-kringle human angiostatin in tumor cells can inhibit both s.c. and metastatic tumor growth of B16F10 melanoma cells. We found that the four-kringle angiostatin suppressed tumor growth in mice in a dose-dependent manner but inhibition was ultimately overcome by the outgrowth of cancer cells with strongly diminished angiostatin expression.
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MATERIALS AND METHODS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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chain secretion signal (METDTLLLWVLLLWVPGSTGDAA-V98). The amino acid sequence of angiostatin started with Val98 of human plasminogen, as described previously (14
, 15)
, and included kringle domains 1–4 of human plasminogen. A similar cDNA encoding murine angiostatin with a HA3
tag (YPYDVPDYA) at the COOH terminus was also synthesized. A CMV promoter drove plasmid-based expression of angiostatin.
Expression of Angiostatin in 293 Cells.
The secretion of angiostatin into the cell culture medium was demonstrated with the vector encoding HA-tagged murine angiostatin. Subconfluent 293 human embryonic kidney cells were transiently transfected on a 100-mm dish with a mix of 10 µg of plasmid DNA and 30 µl of LipofectAMINE in 5 ml of Opti-MEM medium (Life Technologies, Inc, Gaithersburg, MD). After 4 h, the transfection medium was aspirated and replaced with DMEM:F12 (1:1) + 10% FBS. Cells were cultured for 48 h, and medium was collected for Western blot analysis. Attached cells were washed with 1x PBS and lysed in 2 ml of 100 mM sodium phosphate buffer (pH 7.2), 150 mM NaCl, 1% Triton X-100, 20 mg/liter phenylmethylsulfonyl fluoride, 20 mg/liter aprotinin, 20 mg/liter leupeptin, and 2 mg/liter pepstatin.
Western Blot Analysis of HA-tagged Angiostatin Protein.
Rabbit polyclonal anti-HA antibody (2.5 µg; Santa Cruz Biotechnology, Santa Cruz, CA) and 50 µl of protein A/G-Sepharose (Santa Cruz Biotechnology) were added to either 1 ml of conditioned culture medium or 0.5 ml of cell extract and incubated on ice for 1 h. The antibody-Sepharose complex was spun down, washed twice in lysis buffer, and denatured at 95°C in loading buffer. After separation on an 8% SDS-polyacrylamide gel, proteins were transferred to a polyvinylidene difluoride membrane (Amersham, Arlington Heights, IL). Angiostatin was detected with a mouse monoclonal anti-HA antibody (Boehringer Mannheim, Indianapolis, IN) diluted to 5 µg/ml in PBS + 0.1% Tween 20 (TPBS). After washing with TPBS, membranes were incubated with a horseradish peroxidase-coupled secondary antibody (Amersham). Blots were developed with the Pierce Supersignal chemiluminescence system (Pierce, Rockford, IL).
Stable Clones of B16F10 that Overexpress Untagged Human Angiostatin.
Subconfluent B16F10 cells were cotransfected with both the angiostatin expression vector (pMB0388) and a RSVneo expression vector using LipofectAMINE (Life Technologies, Inc.). Transfected cells were selected at 2 mg/ml G418 in MEM containing 10% FBS + nonessential amino acids for 2 weeks. The mass culture was split and cultured with G418 at a lower density for an additional 2 weeks. Single cell clones were picked and expanded in the presence of G418. The cell pellets were then prepared for the analysis of angiostatin mRNA expression.
Detection of Angiostatin mRNA by Quantitative RT-PCR using the Taqman Method.
Total RNA was isolated from cell pellets or tumor samples with the BIO101 FastRNA kit (Vista, CA). Samples were homogenized in FastRNA green tubes filled with 0.5 ml of RNA stabilizing reagent, 0.5 ml of phenol (pH 4), and 0.1 ml of chloroform/isoamyl alcohol. Tubes were placed on ice for 5 min and spun in an Eppendorf centrifuge at 14,000 rpm for 15 min. After a second chloroform/isoamyl alcohol extraction, RNA was precipitated with isopropanol and redissolved in 50 mM Tris (pH 7.4), 10 mM MgCl2, and 10 units of DNase (Boehringer Mannheim). After 1 h, 0.5 ml of RNA stabilizing reagent (FastRNA kit) was added and mixed with 0.5 ml of chloroform/isoamyl alcohol. Finally, RNA was precipitated with isopropanol and redissolved in H2O. Angiostatin mRNA expression was measured by PCR with the Taqman method (19)
and the ABI prism 7700 sequence detection system (Perkin-Elmer Biosystems, Foster City, CA). To assure specific detection of the transgene mRNA without interference from an endogenous mRNA source, the transgene expression vector was designed to transcribe a mRNA with a unique 5'-untranslated region. A synthetic intron splice junction within the untranslated region was the target sequence for the quantitative PCR. Amplification of the angiostatin mRNA was compared with the amplification of standards, and absolute copy numbers were determined with a standard curve. To normalize transgene mRNA concentrations, angiostatin expression is reported as the number of transgene mRNAs per 1,000 copies of endogenous actin mRNA. RT-PCR reactions were started with an initial reverse transcription step at 48°C for 30 min. After denaturation at 95°C for 10 min, PCR was started at 60°C for 1.5 min and completed at 95° for 15 s. The two-step PCR reaction was repeated 39 times. RT-PCR mixture consisted of 100 ng of RNA in a mixture of 8% glycerol; 1x Taqman buffer; 5.5 mM MgCl2; 0.3 mM dATP, dCTP, and dGTP; 0.6 mM dUTP; 1.25 unit of Taq Gold (PE Biosystems); 12.5 units of Moloney murine leukemia virus reverse transcriptase (Life Technologies, Inc., Grand Island, NY); 20 units of RNase inhibitor (PE Biosystems); and primers for either the transgene mRNA (5'-GCTACAGAAGTTGGTCGTGA-3' and 5'-ATGTCGAGAATTCGTCGGCG-3') or murine actin mRNA (5'-AGGTCATCACTATTGGCAACGA-3' and 5'-CACTTCATGATGGAATTGAATGTAGTT-3'). Every PCR reaction also contained 200 nM of a 5'-untranslated probe (6FAM-5'-TGGGCAGGTGTCCACTCCCAGGTT-3'-TAMRA for the quantitation of angiostatin and 6FAM-5'-TGCCACAGGATTCCATACCCAAGAAGG-3'-TAMRA for the quantitation of murine actin; both purchased from PE Biosystems) for transcript quantification.
s.c. and Metastatic Tumor Growth of B16F10 Cells Injected into Syngeneic Mice.
B16F10 cells (1 x 106) in 100 µl of sterile PBS were implanted into the flank of C57BL/6 mice, and the growth of s.c. tumors was monitored. Tumor volume was determined with a Metler digital caliper and calculated using the formula width2 x length x 0.5. The length was taken at the base of the tumors between the two most distant points of the tumor mass, whereas the width was measured right-angled to the length. All measurements were performed on individual animals and then used to calculate tumor volume and tumor frequency per group. To generate metastatic tumors in the lung, either 5 x 104 or 2.5 x 105 B16F10 cells in 0.2 ml of saline were injected into the tail vein of C57BL/6 mice. The number of black nodules on the lung surface was counted after 26 days.
MTT Assay.
To determine cell growth in vitro, B16F10 cells were plated at 10,000 cells/well on a 96-well plate. Cells were grown in MEM + 10% FBS + nonessential amino acids. Cell numbers were determined at 24-h intervals by replacing the culture medium with 0.1 ml of a MTT solution in serum-free DMEM without phenol red [0.5 mg of MTT (Sigma, St. Louis, MO) per ml]. Cells were incubated at 37°C for 2 h, and then 200 µl of solubilizer solution (80% isopropanol, 20% DMSO, and 4% Tween 20) were added to each well. After mixing, absorbance was determined at 562 nm with a plate reader.
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RESULTS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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chain secretion signal. A HA-tag was added to the COOH terminus of the murine protein. Intracellular production of HA-tagged murine angiostatin and the secretion of the protein into the cell culture medium were investigated after transient transfection of 293 cells with the expression construct. Cell culture medium and protein extracts were collected 24 h after transfection and analyzed by immunoblotting. Western blot analysis with an anti-HA antibody revealed that a Mr 50,000 angiostatin protein was produced and accumulated within the cells (Fig. 1A)
. Angiostatin was also secreted into the cell culture medium (Fig. 1B)
. The protein was not detected in B16F10 cells transfected with an expression vector for green fluorescent protein or in immunoprecipitations with an anti-Flag control antibody (Fig. 1, A and B)
. Sequence analysis of the secreted angiostatin protein at the NH2 terminus showed that the immunoglobulin chain signal peptide was cleaved correctly (data not shown).
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Expression of Human Angiostatin cDNA Does Not Inhibit Tumor Cell Growth in Culture.
The specificity of angiostatin for antiangiogenic inhibition of tumor growth, as opposed to a direct inhibition of B16F10 cell growth, was investigated. To address the question, a G418-selected B16F10 cell clone that did not express angiostatin, a clone with high angiostatin expression (3719 RU), and parental B16F10 cells were seeded in 96-well plates, and cell growth was determined using the MTT cell proliferation assay. The three cell lines exhibited the same growth rate (Fig. 2)
. Thus, the expression of the angiostatin transgene does not intrinsically inhibit the growth of B16F10 cells.
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). At the same time, tumors also developed in mice implanted with B16F10 cells that exhibited low angiostatin transgene expression (Fig. 3A)
. However, tumors grew at a slower rate in this group than in the control groups. Subsequently, tumors were found in mice implanted with B16F10 cells that had medium angiostatin transgene expression (Fig. 3, A–C)
. The last group of mice to develop tumors carried the B16F10 cell clone with the highest angiostatin transgene expression (Fig. 3, A–C)
. Thus, angiostatin reduced tumor frequency (Fig. 3A)
and volume (Fig. 3B)
in a dose-dependent manner, and the inhibition was statistically significant (Fig. 3C)
. To examine whether these B16F10 transfectants became resistant to the effect of angiostatin, mRNA concentrations were measured in tumor samples from the angiostatin-expressing clones. Transgene mRNA concentrations were significantly reduced in all tumors and varied from 0.35–1.6% (n = 18) of the mRNA concentration found in the three angiostatin-expressing cell clones before injection into the mice. The results indicate that angiostatin inhibition of tumor growth of B16F10 melanoma cells is directly proportional to the transgene expression and that expression of angiostatin can select for non-angiostatin-expressing tumor cells.
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. None of the animals that received the angiostatin-expressing cells developed more than 3 nodules/lung, and the few nodules that developed expressed less than 1% of the transgene mRNA level found in the same cells before injection. In contrast, 50% of the mice that received the vector control-transfected B16F10 cells had more than 150 nodules/lung. The experiment was repeated with 5 x 104 cells/mouse and 10 animals/clone, and similar results were obtained (data not shown). The significant difference in metastatic growth was not triggered by divergent growth properties of the two cell clones because both clones had the same growth rate in the MTT proliferation assay (Fig. 2)
.
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DISCUSSION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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As a first step toward the use of human angiostatin as a plasmid-based gene therapeutic, we have tested a plasmid construct carrying a CMV-driven transgene encoding a secreted, kringle 1–4 human angiostatin. We specifically chose to express a four-kringle angiostatin instead of a smaller, three-kringle protein because stable expression of a transgene encoding kringles 1–4 of murine angiostatin was found to be a potent inhibitor of tumor growth in mice (16)
. It was also shown that kringle 4 is required for inhibition of endothelial cell migration by angiostatin (15)
. However, the antitumor effect of a cDNA that encoded only kringles 1–3 of human angiostatin has recently been reported (18)
, suggesting that inhibition of endothelial cell migration may not be essential for the tumor suppressor activity of angiostatin. To achieve secretion of the angiostatin protein after gene delivery, we fused the angiostatin cDNA sequence in-frame with a cDNA sequence encoding the murine immunoglobulin chain secretion signal. Although we did not select the plasminogen secretion signal used by others (16, 17, 18)
, a protein sequence analysis of secreted angiostatin showed that the immunoglobulin chain signal peptide was correctly cleaved and assured that secreted angiostatin did not have extra amino acids that could potentially trigger an immune response or hinder activity. Immunoblotting experiments detected a secreted, Mr 50,000 protein after transient transfection of 293 cells with a plasmid encoding the HA-tagged version of angiostatin. Proteolytic digestion of plasminogen was found to produce a Mr 38,000 angiostatin peptide (3)
, but other investigators reported a larger size, ranging from Mr 50,000–58,000, for recombinant four-kringle angiostatin (16
, 20
, 21)
. Thus, our results indicate that the engineered angiostatin protein was correctly secreted upon transgene expression in mammalian cells.
Previous studies showed that angiostatin protein selectively inhibited proliferation of endothelial cells but not of other cell types, including tumor cells (3 , 16) . We similarly found that expression of a high, constitutive level of untagged human angiostatin had no direct effect on tumor cell growth in culture. Expression of angiostatin in the B16F10 cells did not completely block s.c. and metastatic B16F10 tumor growth in mice but prolonged survival by significantly slowing tumor growth. Similar effects on tumor growth were obtained with angiostatin-transfected T241 fibrosarcoma cells (16) and after transduction of human cancer cells with retroviral (17) and adenoviral (18) vectors that carried the angiostatin transgene.
The suppression of primary B16F10 melanomas correlated directly with transgene expression levels. This was observed in repeated experiments. A relationship between angiostatin expression level and tumor growth inhibition has not been described previously. The level of transgene mRNA expression was notably high in the stable transfected cells and ranged from 50–370% of the endogenous -actin mRNA concentration. Because a relationship between angiostatin mRNA abundance and tumoristatic activity was still encountered at this level of transgene expression, our data suggest that a high angiostatin expression level is needed to achieve tumor remission. In comparison, inhibition of primary tumor growth required the administration of 50–100 mg/kg/day of purified angiostatin (12
, 13
, 20)
and was not seen below 10 mg/kg/day (13)
, whereas metastatic tumor was already affected at a dose of 1–2 mg/kg/day (13
, 20)
.
Growth inhibition of angiostatin-transfected B16F10 tumors was transient and coincided with a dramatic decrease of angiostatin expression in those tumors. Escape from dormancy was also observed with angiostatin-transfected fibrosarcomas (16) . It is possible that promoter silencing or a loss of the transgene could have led to the drop in transgene expression in the B16F10 tumors. B16F10 cells are genomically unstable (22) , which could explain a loss of the transgene. Because genomic instability is found in many cancers, the gene therapeutic use of angiostatin may therefore require either repetitive delivery of the cDNA or selective transgene expression in genomically stable tumor endothelial cells to prevent the regrowth of tumors. Cationic liposome-plasmid DNA complexes have been shown to specifically target endothelial cells in tumors (23 , 24) and may be used to deliver a plasmid-based expression vector. For optimal clinical benefits, plasmid DNA therapeutics could also be used in combination with established treatment procedures. An additive effect between angiostatin therapy and ionizing radiation has already been demonstrated (25) .
In summary, expression of an angiostatin transgene can inhibit the growth of a melanoma cell line in mice, and delivery of angiostatin by gene therapy may offer a new opportunity to counter the growth of cancers that have been resistant to current cancer therapies, such as metastatic melanomas.
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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1 Present address: ARIAD Pharmaceuticals, 26 Landsdowne Street, Cambridge, MA 02139. 
2 To whom requests for reprints should be addressed. Present address: ARIAD Pharmaceuticals, 26 Landsdowne Street, Cambridge, MA 02139-4234. Phone: (617) 494-0400, ext. 343; Fax: (617) 252-0851.
3 The abbreviations used are: HA, hemagglutinin; CMV, cytomegalovirus; RT-PCR, reverse transcription-PCR; FBS, fetal bovine serum; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; RU, relative unit(s).
Received 6/ 4/99. Accepted 9/22/99.
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REFERENCES |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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), G418-selected vector control cells (
), and a B16F10 cell clone with high angiostatin expression (3719 RU; 
) were seeded in 96-well plates with 10,000 cells/plate, and cell growth was monitored for 5 days using the MTT proliferation assay. One RU = 1 copy of angiostatin mRNA/1,000 copies of murine actin mRNA. All values represent the arithmetic mean of four replicates; mean + SD is shown for the B16F10 cells with high angiostatin expression, whereas the mean - SD is shown for the G418-selected vector control cells.
) and a clone with a high angiostatin expression level (3719 RU; 
) were injected into the tail vein of C57BL/6 mice (2.5 x 105 cells/animal; 10 mice/group). The number of lung nodules was counted 26 days later. None of the animals died before the analysis.