Gene therapy for carcinoma of the breast: Genetic toxins

bcr25 BCJ Review Gene therapy for carcinoma of the breast: Genetic toxins Vassaux Georges g.vassaux@icrf.icnet.uk Lemoine Nick R

ICRF Molecular Oncology Unit, Imperial College School of Medicine, London, UK

Breast Cancer Res 1465-5411 2000 2 1 22 27 http://breast-cancer-research.com/content/2/1/022 10.1186/bcr25 11178148 17 12 1999 2000 Current Science Ltd cancer gene therapy suicide gene

Abstract

Gene therapy was initially envisaged as a potential treatment for genetically inherited, monogenic disorders. The applications of gene therapy have now become wider, however, and include cardiovascular diseases, vaccination and cancers in which conventional therapies have failed. With regard to oncology, various gene therapy approaches have been developed. Among them, the use of genetic toxins to kill cancer cells selectively is emerging. Two different types of genetic toxins have been developed so far: the metabolic toxins and the dominant-negative class of toxins. This review describes these two different approaches, and discusses their potential applications in cancer gene therapy.

bcr-2-1-022 Gene therapy for carcinoma of the breast David Curiel

Introduction

The first demonstration of the use of controlled expression of an exogenous gene encoding a toxin as a mean of killing cancer cells was described in 1986 [1]. In those experiments, a direct suicide gene (the diphtheria toxin A chain) was used. Extrapolated to a clinical scenario, the use of such a potent genetic toxin (a single diphtheria toxin A chain molecule is capable of killing a cell) would require efficient and very reliable selective targeting of cancer cells. This targeting can be achieved by targeted delivery [2] or by transcriptional targeting [3]. For breast cancer gene therapy, a few promoters have already been used to drive the expression of genetic toxins (Table 1). With current tools, however, accurate targeting cannot be achieved. To accommodate these safety issues, a whole branch of cancer gene therapy has been dedicated to the design of more controllable and specific genetic toxins. These new 'suicide' genes can be classified into two groups: the metabolic suicide genes and the dominant-negative class of suicide genes. This review describes the rationale of these suicide systems and presents their potential applications in breast cancer therapies.

Metabolic suicide gene systems

This strategy relies upon intracellular conversion of a relatively nontoxic prodrug into a toxic drug by an enzyme of xenobiotic origin, and has been referred to as genetic prodrug activation therapy (GPAT). Plant, fungi, bacteria and viruses often utilize unique metabolic pathways that are adapted to their life cycles and environments. These metabolic routes are not used by mammalian cells. In the case of pathogen infections, the distinctive enzymes responsible for these functions have been the target of prodrugs that are developed to be selectively metabolized in infected cells, leading to their destruction. This process is selective, because the prodrug is not toxic to healthy, uninfected mammalian cells.

The transfer of the genes encoding these enzymes to mammalian cells is sufficient to confer sensitivity to particular prodrugs that are metabolized by the individual enzymes. In terms of cancer gene therapy, the process would involve targeted delivery of these genes to the cancer cells, followed by the administration of the prodrug. Compared with a more direct approach, using a suicide gene such as the diphtheria toxin A chain, this prodrug-enzyme system offers extra levels of control, in terms of variation of prodrug concentration as well as prodrug bioavailability and tissue distribution.

Examples of enzyme-prodrug systems

The most suitable enzymes are monomeric proteins, without any requirement for glycosylation. More complex enzymes may not be correctly folded in an ectopic environment and, as a result, may be less efficient at converting the prodrug. This conversion should be rapid [high coefficient of catalysis (K_cat)] and should require low concentrations of prodrug [low Michaelis-Menten constant (K_m)]. In addition, the prodrug should be at least two orders of magnitude less toxic than the active anabolite.

Several enzyme-prodrug systems have been reported (Table 2), and some of these are described below.

Herpes simplex virus thymidine kinase

Ganciclovir and acyclovir are guanosine analogues that are poorly metabolized by mammalian cellular thymidine kinases. By contrast, herpes simplex virus thymidine kinase (HSV-TK) metabolizes these prodrugs very efficiently to their monophosphate forms (the rate-limiting step). In turn, the monophosphate form is metabolized to ganciclovir diphosphate and triphosphate by cellular enzymes. The triphosphate form of the prodrug inhibits α -DNA polymerase [4] and is incorporated into DNA, resulting in chain termination during replication [5]. This molecular mechanism of action implies that this enzyme-prodrug system will only be effective for actively dividing cells and should not affect quiescent cells within a tumour. This view has been challenged by the observation that this system induces significant cell death in tissues with low mitotic indices, however [6]. In these cases, the mechanism of action is unclear and seems to involve a p53-independent apoptosis [6]. Very recently, a library of mutants of HSV-TK was created, from which a more effective form of the enzyme (mutant 30) was described [7]. This type of approach could be applied to improve the characteristics of other enzymes.

Cytosine deaminase

Cytosine deaminase (CD) is an enzyme of bacterial or fungal origin that is activated in response to nutritional stress, deaminating cytosine to uracil. This enzyme became a target for therapy and the prodrug 5-fluorocytosine was selected. 5-Fluorocytosine is metabolized to 5-fluorouracil by CD. Further metabolism of 5-fluorouracil to 5-fluorouridine-5' -triphosphate and 5-fluoro-2' -deoxyuridine-5' -monophosphate results in cell death by affecting RNA and DNA synthesis. The cytotoxic action of CD/5-fluorocytosine requires the proliferation of the target cell. Moreover, 5-fluorouracil is used as a single agent in a limited number of cancers (gastrointestinal tract, for example). Potential problems have been associated with the use of 5-fluorouracil, however, such as the high doses necessary to achieve cytotoxicity and resistance [8,9].

Nitroreductase

Nitroreductase is a monomeric enzyme that converts non-toxic monofunctional alkylating agents to their difunctional forms. The products of these reactions are four orders of magnitude more toxic than the substrates [10]. Escherichia coli nitroreductase has been used to metabolize the prodrug 5-(aziridin-1-yl)-2,4-dinitrobenzamide to 5-(aziridin-1-yl)-4-(hydroxyamino)-2-nitrobenzamide, in the presence of cellular nicotinamide adenine dinucleotide, reduced form, or nicotinamide adenine dinucleotide phosphate, reduced form, acting as a reductant. The metabolized prodrug is then acetylated to 5-(aziridin-1-yl)-4-(acetylamino)-2-nitrobenzamide, which is capable of cross-linking cellular DNA, resulting in apoptosis. This system offers a large number of potential prodrugs that may be optimized. The prodrug currently used in conjunction with nitroreductase is CB1954 [11]. This system offers an advantage over HSV-TK and CD, in that it does not require cell proliferation to induce cell death.

Linamarase

Linamarase is a plant gene that hydrolyzes the cyanogenic glucoside substrate linamarin into glucose, acetone and cyanide. To date, a single study [12] has described the use of this enzyme for GPAT applications, but the originality of this system resides in the fact that the toxic component resulting from the conversion of the prodrug is a gas (cyanide) that can freely diffuse into the adjacent cells, inducing a strong bystander effect. Using this system, the eradication of very large intracerebral gliomas was reported in an animal model [12]. Furthermore, no appreciable toxic effects were observed. Further studies will be necessary to assess the real potential of this GPAT strategy.

Bystander effect

Antitumour gene therapy using GPAT strategies should, in theory, be limited to the cells that have been transduced with the suicide genes. Many investigators, however, have reported the induction of cell death in untransduced tumour cells. This phenomenon, referred to as the 'bystander effect', renders GPAT unexpectedly more efficient than initially predicted. For most of the suicide genes/prodrugs, the molecular mechanisms of this bystander effect have now been characterized, and can be divided into chemical and immunological bystander effects. In vivo, both of these effects may be observed within the same experiment, but with different kinetics.

Chemical bystander effect

One of the first observations of this phenomenon was reported by Culver et al [13]. In these experiments, rat glioma cells were transduced with a replication-deficient retrovirus carrying the HSV-TK gene. Although only 10-70% of the tumour cells were transduced, very significant or complete tumour ablation was observed. Another study [14], with mixed tumour experiments, reported that 10% of HSV-TK-positive cells were sufficient in certain cases to observe tumour regression after treatment with ganciclovir [14]. A very elegant study [15] demonstrated that this bystander effect was the result of a metabolic cooperation, in which molecules of low molecular weight passed from one cell to another through gap junctions. In those experiments, the same cell line was transduced with either HSV-TK or the LacZ gene. When these cells were cocultured at low density, in which the majority of the cells were not in contact with each other, only the HSV-TK-expressing cells died. When the same experiment was repeated in conditions in which the cells were in contact, both cell lines were killed by the action of ganciclovir. These studies strongly suggested that phosphorylated ganciclovir may enter adjacent cells via the gap junction and cause cell death. Another study [16] attributed this bystander effect to the phagocytosis of apoptotic vesicles containing HSV-TK and metabolized ganciclovir, derived from dying cells.

Similar bystander effects were reported with other suicide genes/prodrugs, but the mechanism of toxicity varies among the different agents. For example, it has been shown [17] that 5-fluorouracil can diffuse to nearby tumour cells and pass through the cell membrane. A cell permeable metabolite is also responsible for the bystander effect observed with nitroreductase/CB1954 [18]. In the case of linamarase/linamarin, the cyanide gas produced freely diffuses from one cell to another [12].

Immunological bystander effect

The introduction of the HSV-TK gene into tumour cells, followed by the administration of ganciclovir in vivo, has also been demonstrated, in some cases, to induce the generation of a T-cell dependent antitumour immunity [19,20,21]. For example, Kianmanesh et al [21] demonstrated the existence of a 'distant' bystander effect; HSV-TK-positive or -negative malignant cells were seeded simultaneously in different rat liver lobes, in such a manner that there was no contact between the resulting tumours. After treatment of the rats with ganciclovir, both HSV-TK-positive and HSV-TK-negative tumours regressed and showed infiltration with macrophages and T lymphocytes. Protective immunity to the wild-type tumour was also induced when CD/5-fluorocytosine was used [22,23].

An important parameter that influences this immunological bystander effect is the way in which tumour cell death is induced. Apoptosis is usually associated with cell death in normal developmental processes [24], whereas cell death by a nonapoptotic pathway can be seen as a 'danger' signal (in viral-induced tissue lysis for example), and therefore is more likely to stimulate a immune response. HSV-TK/ganciclovir-mediated tumour killing can occur via apoptotic or nonapoptotic mechanisms, and experimentally the mechanism of HSV-TK-induced cell death can be diverted from apoptosis to nonapoptosis by manipulating intracellular levels of Bcl-2 [25]. Using this system, Melcher et al [25] demonstrated that HSV-TK-induced cell death by a nonapoptotic mechanism was associated with much higher immunogenicity than when tumour death was induced via an apoptotic pathway.

Intriguingly, a 'distant' bystander effect was reported [26] in a plasmacytoma model, when human tumour cells were transferred to severe combined immunodeficient mice. In these mice, a DNA-dependent protein kinase involved in immunoreceptor gene recombination is deficient. This genetic defect causes a complete absence of functional T as well as B lymphocytes. That study suggested that inflammatory cells or natural killer cells might participate in the distant bystander effect observed in immunocompetent animals.

Genetic prodrug activation therapy clinical trial for breast cancer

To date, only one phase I clinical trial using GPAT as a potential treatment for breast cancer has been described [27]. The purpose of the trial was to test the safety and efficacy of tumour-specific expression of the CD gene driven by the erbB-2 promoter. The erbB-2 oncogene is overexpressed in 20% of breast carcinomas and is associated with reduced relapse-free and overall patient survival [28]. Twelve breast cancer patients received the transcriptionally targeted CD gene using direct, intratumoural injection of plasmid DNA, combined with systemic administration of the prodrug. The approach was shown to be safe and resulted in targeted expression of the CD gene in 90% of cases. Significant levels of expression of the suicide gene were detected and this expression was restricted to erbB-2-positive tumour cells. No significant, macroscopically observable tumor regression was reported, however. As a proof of principle, that study demonstrated the feasibility of exploiting transcriptional targeting to drive the expression of suicide genes.

Dominant-negative class of suicide genes

Many studies have been dedicated to the identification of the genetic defects that are associated with the formation and progression of tumours. Among these genetic abnormalities, activating mutations in the ras oncogenes contribute to around 30% of human malignancies [29]. In laboratory experiments, constitutive activation of the Ras signalling pathway has been identified as essential for cellular transformation [30]. Although Ras has clearly been implicated as an inducer of apoptosis in some cellular systems [31], its role in carcinomas and myeloid cells is clearly to protect the transformed cells from apoptosis by inducing, in these cells, a strong survival signal [31]. This survival pathway triggered by Ras activation has been partly characterized and encompasses phosphatidyl inositol-3 kinase [32] and the protein serine/threonine kinase akt, also known as the protein kinase B [33]. These findings suggest that disruption of Ras function may be an effective approach in the treatment of carcinomas.

The elucidation of the Ras signalling pathway was made possible partly because of 'dominant-negative' proteins. These proteins are mutated versions of natural proteins and act as terminators of signalling pathways. For example, the dominant-negative Ras N116Y was created from the v-H-ras oncogene by substitution of tyrosine for asparagine at codon 116 [34]. This mutation leads to the destruction of the guanosine triphosphate-binding site and results in a catalytically inactive enzyme that can nevertheless bind to downstream elements of the signalling pathway. The dominant-negative will then compete with the normal Ras and may totally block the pathway. Using this approach, it was demonstrated that transfection of Ras N116Y to various human cell lines of malignant origin resulted in growth inhibition in vitro [35]. These results were expanded in vivo, when two oesophageal cell lines, containing a mutant Ras or a wild-type Ras, were used to seed tumours in nude mice [36]. The animals then received a treatment that consisted of repeated injections of adenovirus carrying the dominant-negative Ras N116Y driven by the cytomegalovirus promoter. The treatment significantly reduced the growth of both cell lines in vivo, without any noticeable adverse effects. That study is, to our knowledge, unique thus far as it demonstrates the clinical potential of this strategy. Moreover, the elucidation of the complete Ras signalling pathway could give rise to a growing number of dominant-negative genes that could be used in conjunction to block the survival pathway.

Conclusion

Since the first experimental demonstration showing efficient killing of cells by a transfected gene encoding diphtheria toxin A chain, a variety of new genetic toxins have been designed and tested in preclinical studies. The first clinical trial of GPAT for breast cancer has just been completed, and demonstrated the safety and feasibility of the strategy. The long-term success of GPAT systems for clinical treatment of cancer will rely on the development of efficient and targeted gene therapy systems, however. This targeting can be achieved in two ways: targeted delivery, in which the gene medicine will be selectively delivered to the tumour cells; and transcriptional targeting, which uses promoters that will be active only in tumour cells. Ideally, a combination of both targeting systems will be used.

As an alternative to GPAT, exploitation of the knowledge accumulated on mechanisms adopted by cancer cells to evade programmed cell death could produce genetic toxins such as dominant-negative mutants of the Ras signalling pathway that are more specific to cancer cells and do not need such sophisticated targeting systems. This type of approach is only just being tested, and safety issues remain to be addressed.

Table 1

Promoter constructs that have been exploited for breast carcinoma gene therapy

Promoter construct

Reference

DF3/MUC1 promoter

[37]

ErbB-2 promoter

[3,27**,38]

ErbB-2 promoter/MUC1 enhancer

[39]

Table 2

Enzyme-prodrug systems under investigation for genetic prodrug activation therapy applications

Enzyme

Prodrug

Cytotoxic product

Herpes simplex virus thymidine kinase

Ganciclovir

Ganciclovir triphosphate

Cytosine deaminase

5-Fluorocytosine

5-Fluorouracil

Varicella zoster virus thymidine kinase

6-Methoxypurine arabinose

Adenine arabinonucleoside triphosphate

Nitroreductase

CB1954

5-Aziridinyl-4-hydroxylamino-2-nitrobenzamide

Cytochrome p450

Cyclophosphamide

Acrolein and phosphoramide mustard

Thymidine phosphorylase

5' -Deoxy-5-fluorouridine

5-Fluorouracil

Purine nucleoside phosphorylase

6-Methylpurine-deoxyriboside

6-Methylpurine

Alkaline phosphatase

Etoposide phosphate

Etoposide

Carboxypeptidase A

Methotrexate-alanine

Methotrexate

Carboxypeptidase G2

Benzoic acid mustard-glucuronide

Benzoic acid mustard

Linamarase

Linamarin

Cyanide

Xanthine oxidase

Xanthine

Oxygen radicals

β -Lactamase

Cephalosporin-mustard-carbamate

Nitrogen mustard

Regulated expression of a diphtheria toxin A-chain gene transfected into human cells: possible strategy for inducing cancer cell suicide. Maxwell IF Maxwell F Glode LM Cancer Res 1986 46 4660 4664 3460697 Strategies for targeting therapeutic gene delivery. Peng KW Mol Med Today 1999 5 448 453 10.1016/S1357-4310(99)01579-8 10498913 Gene therapy for cancer using tumour-specific prodrug activation. Harris JD Gutierrez AA Hurst HC Sikora K Lemoine NR Gene Ther 1994 1 170 175 7584078 Insertion and extension of acyclic, dideoxy and ara nucleotides by herpesviridae, human α and β polymerases. A unique inhibition mechanism for 9-(1, 3-dihydroxy-2-propoxymethyl) guanine triphosphate. Reid R Mar EC Huang ES Topal MD J Biol Chem 1988 263 3898 3904 2831212 Inhibition of cellular DNA polymerase α and human cytomegalovirus-induced DNA poly-merase by triphosphates of 9-(2-hydroxyethoxymethyl) guanine and 9-(1, 3-dihydroxy-2-propoxymethyl) guanine. Mar EC Chiou JF Huang ES Topal MD J Virol 1985 53 776 780 254706 2983088 Ganciclovir-induced ablation of non-proliferating thyrocytes expressing herpesvirus thymidine kinase occurs by p53-independent apopto-sis. Wallace H Clarke AR Harrison DJ Hooper ML Bishop JO Oncogene 1996 13 55 61 8700554 Enhancement of tumourablation by a selected HSV-1 thymidine kinase mutant. Kokoris M Sabo P Adman E Black M Gene Ther 1999 6 1415 1426 10.1038/sj.gt.3300966 10467366 Fluorouracil: biochemistry and pharmacology. Pinedo HM Peters GFJ J Clin Oncol 1988 6 1653 1644 3049954 Effect of folinic acid on fluorouracil activity and expression of thymidine synthase. Van der Wilt CL Pinedo HM Smid K Semin Oncol 1992 19 16 25 1532671 The bioactivation of CB 1954 and its use as a prodrug in antiboby direct enzyme prodrug therapy (ADEPT). Knox RJ Friedlos F Boland MP Cancer Metastasis Rev 1993 12 195 212 8375021 Selective cell ablation in transgenic mice expressing <it>E. coli</it> nitroreductase. Clark AJ Iwobi M Cui W Gene Ther 1997 4 101 110 10.1038/sj.gt.3300367 9081700 Successful use of a plant gene in the treatment of cancer <it>in vivo</it>. Cortes ML de Felipe P Martin V Hughes MA Izquierdo M Gene Ther 1998 5 1499 1507 10.1038/sj.gt.3300751 9930303 <it>In vivo</it> gene transfer with retroviral vector-producer cells for treatment of experimental brain tumours. Culver KW Ram Z Wallbridge S Science 1992 256 1550 1552 1317968 Multiple transduction as a means of preserving ganciclovir chemosensitivity in sarcoma cells carrying retrovirally transduced herpes thymidine kinase genes. Moolten FS Wells JM Mroz PJ Cancer Lett 1992 64 257 263 10.1016/0304-3835(92)90051-V 1322236 <it>In vivo</it> evidence that metabolic cooperation is responsible for the bystander effect observed with HSV tk retroviral gene therapy. Bi WL Parysek LM Warnick R Stambrook PJ Hum Gene Ther 1993 4 725 731 8186287 The bystander effect: tumor regression when a fraction of the tumor mass is genetically modified. Freeman S Abboud CN Whartenby KA Cancer Res 1993 53 5274 5283 8221662 Bystander effect caused by cytosine deaminase gene and 5-fluorocytosine <it>in vitro</it> is substantially mediated by generated 5-fluorouracil. Kuriyama S Masui K Sakamoto T Anticancer Res 1998 18 3399 3406 9858915 The bystander effect of the nitroreductase/CB1954 enzyme/prodrug system is due to a cell-permeable metabolite. Bridgewater JA Knox RJ Pitts JD Collins MK Springer CJ Hum Gene Ther 1997 10 709 717 Immune system in suicide gene therapy. Freeman SM Ramesh R Marrogi AJ Lancet 1997 349 2 3 8988108 Generation of an anti-tumour immune response in a non-immunogenic tumour: HSVtk killing in vivo stimulates a mononuclear cell infiltrate and a Th1-like profile of intratumoural cytokine expression. Vile RG Castleden S Marshall J Int J Cancer 1997 71 267 274 10.1002/(SICI)1097-0215(19970410)71:2<267::AID-IJC23>3.3.CO;2-J 9139853 A distant bystander effect of suicide gene therapy: regression of nontransduced tumors together with a distant transduced tumor. Kianmanesh AR Perrin H Panis Y Hum Gene Ther 1997 8 1807 1814 9358030 5-fluorocytosine-induced eradication of murine adenocarcinomas engineered to express the cytosine deaminase suicide gene requires host immune competence and leaves an efficient memory. Consalvo M Mullen CA Modesti A J Immun 1995 154 5302 5312 7730633 Tumours expressing the cytosine deaminase suicide gene can be eliminated <it>in vivo</it> with 5-fluorocytosine and induce protective immunity to wild type tumor. Mullen CA Coale MM Lowe R Blaese RM Cancer Res 1994 54 1503 1506 8137255 Cell death: current difficulties in discriminating apoptosis from necrosis in the context of pathological processes <it>in vivo</it>. Columbano A J Cell Biochem 1995 58 181 190 7673326 Tumor immunogenicity is determined by the mechanism of cell death via induction of heat shock protein expression. Melcher A Todryk S Hardwick N Nature Med 1998 4 581 587 9585232 Suicide gene therapy for plasma cell tumors. Dilber MS Abedi MR Bjorkstrand B Blood 1996 88 2192 2200 8822939 Genetic prodrug activation therapy for breast cancer: a phase I clinical trial of <it>erb</it> B-2-directed suicide gene expression. Pandha HS Martin LA Rigg A J Clin Oncol 1999 17 2180 2189 10561274 c erbB-2 oncoprotein expression in primary and advanced breast cancer. Lovekin C Ellis IO Locker A Br J Cancer 1991 63 439 443 1672254 Ras oncogenes in human cancer: a review. Bos JL Cancer Res 1989 49 4682 4689 2547513 Essential role for oncogenic Ras in tumour maintenance. Chin L Tam A Pomerantz J Nature 1999 400 468 472 10.1038/22788 10440378 Ras signalling and apoptosis. Downward J Curr Opin Genet Dev 1998 8 49 54 10.1016/S0959-437X(98)80061-0 9529605 Role of phosphoinositide 3-OH kinase in cell transformation and control of the actin cytoskeleton by Ras. Rodriguez-Visciana P Warne PH Khwaja A Cell 1997 89 457 467 9150145 Ras effectors. Marshall CJ Curr Opin Cell Biol 1996 8 197 204 10.1016/S0955-0674(96)80066-4 8791426 Mutations of the <it>ras</it> gene product p21 that abolish guanine nucleotide binding. Clanton TJ Hattori S Shih TY Proc Natl Acad Sci USA 1986 83 5076 5080 3014531 Suppression of various human tumor cell lines by a dominant negative H-<it>ras</it> mutant. Ogiso Y Sakai N Watari H Yokohama T Kuzumaki N Gene Ther 1994 1 403 407 7584106 Suppression of Erk activation and in vivo growth in esophageal cancer cells by the dominant negative <it>Ras</it> mutant, N116Y. Senmaru N Shichinohe T Takeuchi M Int J Cancer 1998 78 366 371 10.1002/(SICI)1097-0215(19981029)78:3<366::AID-IJC18>3.0.CO;2-4 9766573 Breast cancer selective gene expression and therapy mediated by recombinant adenoviruses containing the DF3/MUC1 promoter. Chen L Chen D Manome Y J Clin Invest 1995 96 2775 2782 8675647 Insulation of a conditionally expressed transgene in an adenoviral vector. Vassaux G Hurst HC Lemoine NR Gene Ther 1999 6 1192 1197 10.1038/sj.gt.3300910 10455425 Use of transcriptional regulatory elements of the MUC1 and ERBB2 genes to drive tumour-selective expression of a prodrug activating enzyme. Ring CJA Blouin P Martin LA Hurst HC Lemoine NR Gene Ther 1997 4 1045 1052 10.1038/sj.gt.3300510 9415310