A background-lying platform of this work derives from experimental data on magnetic isotope effects (MIE) towards both DNApolβ catalytic activity    and the viability of cancer cells   . Thus, a sharp decrease of the survival ability patterns of 25Mg2+-treated AML/HL-60 cells as compared to abundant spinless, non-magnetic, magnesium ions impact has been found  . Furthermore, a similar result was then obtained on the same leukemia cells treated with magnetic, nuclear spin possessing, 43Ca2+ and 67Zn2+ ions   as well as on human retinoblastoma cells subjected to these metal isotopes   .
It was also shown that a processivity of beta-like DNA polymerases isolated from the all above mentioned malignant cells depends on MIE, so the resulted DNA fragment sizes becomes shorter within a 40n - 250n range following the increase of magnetic isotope content in a total metal pool   . For instance, an up to 58% elevation of 43Ca2+ content leads to a monotonic decrease of sizes of polynucleotides processed from average 230n - 250n to an abnormal (DNA repair invalid) 36n - 40n as directed by beta-like DNA polymerases from Y-79 and WERI-1A retinoblastoma cells  .
This nuclear-magnetic control over the DNA synthesis, therefore, allows coming up with a firm statement that a replication mechanism involves some ion-radical steps consisting of the ion-radical pairs formation  . A key element of this mechanism deals with an electron transfer from the nascent DNA deoxyribose anion to a bivalent ion coordinated inside the DNA polymerase catalytic site   (Figure 1).
However, from the chemical physics point of view, it is still obscure what makes the difference between molecular dynamics designs of these ion-radical DNA synthesis paths processed in healthy and malignant cells. Noteworthy, within the DNApolβ catalytic site nanotopology landscape which provides a
Figure 1. A reaction of electron transfer from the nascent DNA deoxyribose anion to a bivalent metal ion.
“compartment” for this reaction (10 - 15 nm or less), all physical parameters describing a molecular machinery in normal and cancer cells at proliferation rates observed are identical or pretty close to each other  -  .
Obviously, the DNA synthesis reaction    is unlikely a source for apoptosis of tumor cells as relates to dependence of their viability on MIE  . Nonetheless, this MIE-viability dependence might have a link to DNA repair activity expressed by beta-like DNA polymerases in neoplasma    .
According to our assumption, these enzymes are to produce the ultrashort PDRN sequences (≈40n) playing a role of DNApolβ inhibitors. Acting as the DNA repair limiting/damaging factors, these endogenous inhibitors may promote an essential anti-cancer effect. In case of 25Mg/43Ca/67Zn-induced impacts on enzymatic activity in situ, these inhibitors might be originated as a direct response to MIE.
Moreover, due to a random mode of the cancer-specific repair-required local DNA damages, the DNA repair itself means a wide variability in primary structures of the repair-related PDRN species. This also means that the PDRN inhibitory function should be determined predominantly, if not exclusively, by the lengths of these sequences. These lengths alone might determine not only the molecular dynamics in DNApolβ-PDRN docking pairs but, simultaneously, they might make an impact on specific Coulomb and dispersion couplings and, hence, on the mean amounts of hydrogen bonds per one nucleotide of the DNA primer inside the enzyme catalytic site.
So if this assumotion is true, the DNApolβ activity must be “suppressible” by ≈ 40n-long polynucleotides regardless on their primary structures. This would make the MIE-promoting treatment a legitimate may to gain the in situ anti-cancer molecular events.
The aim of a present study is to test this hypothesis. For this purpose, several types of synthetic single-stranded polynucleotides (both DNA- and RNA-like ones) with molecular sizes ranged in 20n - 200n interval were investigated to reveal 1) their effects on catalytic activities of several beta-like DNA polymerases from HL-60, Y-79 and WERI-1A cancer cells, and 2) their enzyme-binding parameters. A selection of these peculiar cell models was determined solely by a sharp difference between the tumor proliferation rates, “aggressive” high (acute myeloid leukemia) and relatively low (retinoblastoma)    and, hence, by the difference in contributions made by the DNA repair key enzymes into the cancer cell survival capabilities.
2. Materials and Methods
2.1. Reagents and Disposal Materials
Aphidicolin (Fluka, Switzerland); ddTTP (Boehringer-Mannheim, Germany); Proteinase K (Serva, Germany); HSA (Sigma, USA); yeast tRNA (Serva, Germany); calf thymus DNA primer (Merk, Germany); dATP, dTTP, dCTP, dGTP (Serva, Germany); dioxane- and toluene-based media for liquid beta-scintillation count MS460 and MS710 (Merk, Germany); CS20 25 mm fiberglass filters (Millipore, France); AccuPrep DNA extraction K2600 kit (Bioneer, Rep. Korea); [Methyl-1,2-3H]dTTP, 120 - 160 Ci/mmol (Amersham, UK).
Poly(dT)25, Poly(dT)50, Poly(dT)100, Poly(dT)200 (ThermoFisher, USA); Poly(A)49, Poly(2-thio-dC)49, Poly(dT)40 (IBC RAS, Russia); Poly(dT)40, Poly(dT)80 (ICBFM RAS, Russia); Poly([2-14C]CN-dT)40, 20 - 38 Ci/mmol; Poly([2-14C]CN-dT)80, 20 - 32 Ci/mmol; Poly([5-14C]CN-dT)40, 18 - 24 Ci/mmol; Poly([5-14C]CN-dT)80, 16 - 22 Ci/mmol (Perkin Elmer, USA).
PAGE-homogenous beta-like monomeric, 66.5 kDa and 23.5 kDa, DNA polymerases (EC 126.96.36.199) purified from chromatine of HL-60 acute myeloid leukemia cells  and WERI-1A, Y-79 retinoblastoma cells  were employed. Thus, to purify these chromatine-associated DNA repair programming enzymes, the following   —promoted technique has been used. First, the chromatin fraction of the cell lysate was obtained. For this purpose, the protein containing crude nuclei phenol-chloroform extracts   were mixed with 10 volumes of an ice-cold acetone and kept at +4˚C overnight. An acetone-insoluble material was precipitated at 20,000 rpm, 20 min, +4˚C. The pellets were extensively re-washed with acetone using the same procedure and then dissolved in 5 - 6 volumes (w/v) of 25 mM potassium-phosphate (pH 6.30)/0.5% NaCl/1.5 mM EDTA/0.01% glutathione/0.05% heparin/1.0% 2-mercaptoethanol/80 - 100 U/mL nuclease S followed by 40 min incubation at +37˚C. All post-incubation mixtures were treated by sonication at 80 KHz, 30 min, +60˚C, under a non-stop extensive shaking. Then these mixtures were submitted to a scalar fractionation path reaching the 30% - 70% ammonium sulfate saturation, consequently. The precipitates obtained were collected at 10,000 rpm, 20 min, and dissolved in 15 mM potassium phosphate buffer (pH 6.0)/0.2% NaCl (10 vols, w/v). The solutions were subjected to dialysis against 20 mM potassium phosphate buffer (pH 6.0) and lyophilized.
The lyophilized powders were first dissolved in 15 mM potassium phosphate (pH 6.30)/5.0 mM MgCl2/1.5 mM EDTA/0.0001% sodium azide and passed through the fiberglass filters with 0.3 - 0.4 μ pore diameter (Millipore 5R, Millipore, France). The transparent solutions were subjected to ultrafiltration on membranes with the molecular size exclusion limit of 5.0 kDa at 800 p.s.i. (Diaflo Y5.0 25 mm membranes, Amicon BV, The Netherlands). The membrane-re- tained material was then extracted with 10 mM Tris-HCl (pH 8.0)/1.0% 2-mer- captoethanol (v/v), 5.0 mL per a razor-disintegrated membrane, +30˚C, 12 hrs, with a following concentration in a rotor evaporizer.
The 1.5 - 2.5 mL samples were then applied onto a 1.5 × 50 cm (V = 98 mL) column packed with the TOYOPEARL HW 55F gel and equilibrated by the eluent buffer consisting of 15 mM potassium phosphate (pH 6.30)/5.0 mM MgCl2/ 0.0001% sodium azide. Elution rate: 0.8 mL/min (room temperature). In each one of the consequently eluted 1.5 mL fractions, the DNA polymerase activity has been measured according to   .
2.4. Enzyme Activity Estimation
Beta-like catalytic activity values were expressed in amounts of [3H]dTTP incorporated into nascent DNA chains in 1 min of incubation at optimal conditions corrected per 1.0 mg of pure enzyme protein ([3H]DNAcpm/mg protein) as described in   . The enzyme catalytic activity was measured in 0.15 mL incubation mixtures consisting of 50 mM Tris-HCl (pH 8.0)/8.0mM dithiothreitol/15 mM MgCl2/15% glycerol (v/v)/27 2 μg act DNA, calf thymus/50 μg each of dATP, dCTP, dTTP, dGTP/0.25 μmole [Methyl-1,2-3H]dTTP (90 - 120 Ci/mmol, NET520A, NEN)/150 mM NaCl. The tritium-labeled nucleotide was purchased from New England Nuclear, USA. These compound concentration values were first pre-optimized within both pH 6.0 - 9.0 and 5.0 mM - 50.0 mM MgCl2 ranges. These mixture samples were first pre-incubated at +37˚C for 60 min. Then 5.0 - 7.5 μg of pure enzyme was added to each one of these running samples and they were incubated at +37˚C for 60 min longer. The ice cold incubation samples (0˚C, 60˚C after pre-incubation) as well as the trypsin treated samples (20 μg/mL trypsin, Merck GmbH, Germany, +37˚C, 60˚C) were taken for controls.
The post-incubation mixtures were subjected to a quantitative extraction of the DNA ultramicro-amounts using an AccuPrep Genomic DNA Extraction Kit (Bioneer Corp., Korea).
2.5. DNA and Protein Measurements
The DNA ultramirco amounts measurements were performed in diluted water solutions according to   . The protein ultramicro amounts were estimated by method  modified in  .
2.6. Radioactivity Measurements
For [3H] and [14C] radioactivity quantitative detection, the cpm values were determined using the DNA-retaining fiberglass filters (DNApolβ post-incubation ethanol-precipitation pellets)  placed into dioxan or tolyene media    with a following processing in Wallac 2200LX liquid scintillation counter (Wallac, Finland).
2.7. Ligand-Enzyme Binding Measurements
To quantify a ligand-enzyme binding patterns, a conventional criteria such as Kdis (Kd) and Ac were taken into account.
A Baileyan model was applied for an algorithm leading to a ligand-enzyme (ligand-receptor) dissociation constant estimate   .
In this approach, a ligand-receptor interaction , where R is the receptor, L is the ligand, RL is the ligand-receptor complex, is the probability of formation of a complex molecule, and is the probability of its dissociation. If the random number of ligand-receptor complex molecules is x, and the initial number of receptors is , the number of free receptors makes . Assume that the process unfolds under the condition of large ligand surplus, so that the number of ligand molecules stays equal to its initial value . The formation of ligand-receptor complexes is described by the function , and their decomposition—by . Bailey’s equation system is:
Following this algorithm, an experimental data on the ligand-enzyme complexes stability in water solutions obtained by techniques described in   and modified in  , and affected by temperature/ultrasound/ionic strength were processed using a LQ170 SigmaLab software in HP9000 analytical system (Hewlett Packard, USA).
For a non-specific binding control, HSA and denaturated-renaturated misfolded yeast tRNA were employed as the pseudoligands   .
In all enzyme-ligand coupling tests, the enzyme required optimal catalytic parameters   were held for 40 min, +37˚C, while the following ligand concentrations kept at 0.1 μM, 0.5 μM, 10.0 μM, 20.0 μM, 50.0 μM, as recommended in   .
The UV-spectrophotometry (Lambda 1050 Scanning Spectrophotometer, Perkin Elmer, USA) was employed using the Spectra Manager II cross-platform software (JASCO, USA) for automated data treatment with an aim to gain the Ac index indicating an extent of polynucleotide release from ligand-enzyme in water solution owing to a certain consent of A210, A254, A280 values,  .
A Dunnett’s non-parametric (n ≤ 6) technique was used to elucidate reproductability of the data along with a significance of differences in control-experiment comparisons  .
A variable set of polynucleotide ligands (see Methods) was tested for both inhibitory effects and the ligand-enzyme binding properties using beta-like DNA polymerase species from acute myeloid leukemia (HL-60) and retinoblastoma (WERI-1A, Y-79) cells.
As seen from the data presented in Figure 2 and Figure 3, no matter what ligand concentration tested and whatever enzyme sample coupled, a molecular size of synthetic polynucleotide is the only, crucial, impact-making factor. It should be emphasized that a maximal inhibition effects were observed in cases of 50n - 100n-long polynucleotides (Figure 2(C) and Figure 2(D)), Figures 3(A)-(E)), while a post-denaturation misfolded tRNA test show no inhibition
Figure 2. (A) Catalytic activities of beta-like DNA polymerases from HL-60, WERI-1A and Y-79 cancer cells under optimal and modified incubation conditions. (B) Catalytic activities of beta-like DNA polymerases from HL-60, WERI-1A and Y-79 cancer cells in the presense of Poly(dT)25. (C) Catalytic activities of beta-like DNA polymerases from HL-60, WERI-1A and Y-79 cancer cells in the presense of Poly(dT)50. (D) Catalytic activities of beta-like DNA polymerases from HL-60, WERI-1A and Y-79 cancer cells in the presense of Poly(dT)100. (E) Catalytic activities of beta-like DNA polymerases from HL-60, WERI-1A and Y-79 cancer cells in the presense of Poly(dT)200.
Figure 3. (A) Catalytic activity of AML/HL-60 beta-like DNA polymerase in the presense of Poly(dT)49 and renaturated yeast tRNA. (B) Catalytic activity of AML/HL-60 beta-like DNA polymerase in the presense of Poly(A)49 and renaturated yeast tRNA. (C) Catalytic activity of AML/HL-60 beta-like DNA polymerase in the presense of Poly(thio-dC)49 and renaturated yeast tRNA. (D) Catalytic activity of AML/HL-60 beta-like DNA polymerase in the presense of Poly(dT)40. (E) Catalytic activity of AML/HL-60 beta-like DNA polymerase in the presense of Poly(dT)80.
The affinity isotherms clearly show an essential difference between the ligand-enzyme complex stability patterns, Kd and Ac (see Methods), estimated for numerous compositions of these couples (Figure 4 and Figure 5). Thus, dissociation constant Kd for Poly(dT)50-DNApolβ was found by 2.5-fold smaller as compared to Poly(dT)200-DNApolβ pair (Figure 5).
In all cases studied, except for the RNA-like Poly(A)49-containing pairs (Figure 5), Kd and Ac values are minimal when the ligand length is close to 50n (Figure 6). For all RNA-like ligands, the high values of Kd and Ac were found practically equal to the ones estimated for Poly(dT)200 (Figure 5).
The data presented in Figure 2 and Figure 3 leaves no doubt about a maximal inhibitory efficiency provided by ultrashort, 40n - 50n in length, cyano-polydeoxyribothymidyl derivatives. These agents are to show as high as nearly 6.5-fold extent of enzyme suppression. That does not mean, however, that
Figure 4. Affinity isotherms for HL-60-DNApolβ/Poly(dT)50 (1) and HL-60-DNApolβ/Poly(dT)200 (2) ligand-acceptor complexes. For technical details, see Methods.
Figure 5. Polynucleotide-enzyme binding patterns (Kdis, Ac) estimated for beta-like DNA polymerase species from three cancer cell lines (HL-60, WERI-1A, Y-79). For technical details, see Methods.
this particular type of “pseudoprimers” is the only one capable to play a role of a powerful DNApolβ inhibitor. A truly crucial parameter to reveal a potential pharmacophore signs have nothing to do with a structure of DNA fragments being entirely related to its molecular size (Figure 2 and Figure 3).
So the results observed looks worthy of not indicating to any particular and perfect pharmacophore found but, instead, of a detailed analysis as a new platform to upgrade a whole approach towards the DNA derivatives in a current
Figure 6. (A) A sonication affected stability of the couples of HL-60 beta-like DNA polymerase and 14C-labeled Poly(CN-dT)40 evaluated by detection of free ligand release. For technical details, see Methods. (B) A sonication affected stability of the couples of HL-60 beta-like DNA polymerase and 14C-labeled Poly(CN-dT)80 evaluated by detection of free ligand release. For technical details, see Methods. (C) A salt-caused decay of the unstable complexes between HL-60 beta-like DNA polymerase and 14C-labeled Poly(CN-dT)40 evaluated by detection of free ligand release. For technical details, see Methods. (D) A salt-caused decay of the unstable complexes between HL-60 beta-like DNA polymerase and 14C-labeled Poly(CN-dT)80 evaluated by detection of free ligand release. For technical details, see Methods.
anti-cancer agenda. This a Discussion of our work is all about.
A wide diversity of investigated synthetic homopolynucleotides and their monotonic thio- and cyano-derivatives is itself a prove for universal, indiscriminate, mode of DNApolβ inhibition effect we described. This is in a favor with our assumption stated that the key role in this phenomenon belongs exclusively to molecular sizes of small DNA fragments regardless on their primary structure peculiarities.
The ligands diversity mentioned makes no way to explain a formation of the ligand-enzyme complexes just by a routine docking (“complimentary”) paradigm. This DNA-protein binding act may involve some random appearing hydrogen bonds, Coulomb hyperfine coupling along with dispersion interaction and, last not least, the hydrophobic connections, might also be a case in this scenario. A key point of this model derives from the homopolynucleotides related data and reveals that the mean energy of these “weak” interaction depends on the length of a ligand but not of its structure.
A similar event occurs in the DNA repair process as long as a randomly appeared local DNA damage comes first. In this case, a clearly indiscriminate mode of the ligand-enzyme coupling is a consequence of unpredictable variability in primary structures of DNA fragments suitable for the repair purposes.
Therefore, a polynucleotide length alone is an impact-making factor towards the DNApolβ catalytic function. This factor might determine a formation of the above listed “weak” non-covalent interactions and, hence, to control the mean amount of hydrogen bonds per one nucleotide of DNA-primer (ligand) inside the DNA polymerase catalytic site. That is indeed critical for the enzyme suppression in situ.
All the affinity isotherms presented and a variable ligand-enzyme binding data (Figures 4-6) reveals a maximal strength of this peculiar intermolecular interaction within the short interval of ligand sizes, 50n - 100n. This is to confirm that the enzyme inhibition we observed (Figures 2(B)-(E), Figure 3) is indeed a consequence of the stable ligand-enzyme pair formation which has nothing to do with either the solution properties changes or the enzyme surrounding disperse phase modulations.
A comparison between the ligand amounts bound with (a) DNApolβ and (b) HSA show that the ligand-enzyme complex includes two molecules of ligand per one molecule of enzyme, while the ligand-HSA (control) pair contains just one ligand per HSA molecule (Figure 4, Figure 7, Figure 8). This is in a favor to a mere fact of existance of two separate Mg2+-coordinating catalytic sites in β- and β-like DNA polymerases      .
Figure 7. An activation energy of the ligand-enzyme binding as affected by temperature in DNApolβ-HL60/Poly(dT)50 pair formation. . See Discussion.
Figure 8. Temperature-dependent ligand binding in DNApolβ-HL60/Poly(dT)50 pair. L’—DNApolβ, receptor; L*—HAS, receptor (control). For technical details, see Methods.
dependence of Kd on temperature has a clear Ahrrenius mode:
where R—a universal gas constant and T-enzyme functioning temperature.
Taking into account a low level of the temperature interval tested as compared to an initial T0 = 298K, we’ll use further a linear decay as T in (1). To estimate E, a linear reguliarity must be treated as:
The Equation (2) revealed activation energy value E was found 15 kJ for Poly(dT)200 ligand within a whole range of temperatures tested, while the very same dependence for Poly(dT)50 include two linear branches crossing each other nearby the 40˚C point where, most likely, a slight protein denaturation starts (Figure 7). Once the temperature is close to an enzyme function required optimal level (25˚C - 35˚C), the Equation (2) revealed E50 = 70 kJ/mole whereas this value estimated at 40˚C is as low as 15 kJ/mole (Figure 7). The attention catching point here is that the E value measured at the enzyme denaturation launch-point (40˚C) is exactly the same as it has been found in case of the “inert”, non-inhibiting, polydeoxyribonucleotide ligands. This supports a statement on the enzyme inactivating protein structure dynamics initiated starting with a 40˚C heating point. A lack of two-compartment, “angle-breaking”, dependence for long ligands and their E values low level are in a good accordance with a high probability of 3D-compactization of such sequences at our test conditions     .
It’s easy to find out that the inhibition-promoting Poly(dNTP) species provide a pretty low value of activation energy for dissociation with DNApolβ-HL60, ε = 1.40 kJ/mole. That means, the complimentary hydrogen bonds do not contribute to formation of these particular Poly(dNTP)-enzyme complexes which is a prove for the absence of the affinity-specific, true docking links in these pairs. Most probably, this remarkable 1.40 kJ/mole value is determined by the Ud-dispersion related weak Van der Waals interactions along with a Uq Coulomb hyperfine coupling. These kinds of the ligand-enzyme complex stabilizing links are rather superficial ones due to both a potential and the efficient screen-like separation of Coulomb forces in water occurred within a distance smaller than 0.4 nm     . This certainly takes into account the superficial hydrophobic bounds as well which are nothing but the result of a cooperative (cumulative) act of all the above specified forces   .
So the key role in formation of Poly(dNTP)/DNApolβ complexes belongs to Van der Waals bounds which energy corresponds directly to either 1) the efficient surface of ligand-enzyme pair or 2) a length of an enzyme-bound ligand.
Furthermore, since the mean value of the Ud dispersion patterns is hardly dependent on the element composition, and as long as the amounts of charged groups in Uq-determining Poly(dNTP) ligands tested are about the same, a very similar parameters of their inhibitory activity should be expected then. This explains well a lack of dependence of inhibitory capabilities of these ligands on their nucleotide composition (Figures 2(B)-(E), Figure 3).
Once , we might suppose that the short ligands (50n - 100n, or shorter) are to get bound with the enzyme molecule throughout a whole linear chain, i.e. through nearly every nucleotide of Poly(dNTP) sequence.
Using the Ahrrenius equation, we may evaluate a ratio between the ligand- enzyme binding time values τ for Poly(dNTP)20 and Poly(dNTP)50, respectively:
where (difference in lengths between 50n and 20n). It shows that a short time of binding does not allow n20-ligand to promote a sharp suppression of the enzyme activity. A shorter time for the ligand “neighboring” around the enzyme catalytic site, the lesser inhibitory effect to be expressed.
On other hand, the longest ligands tested were found to be a rather poor inhibitors as well (Figure 2(E), Figure 4) due to their compactization-caused small square of the enzyme-ligand efficient interaction   as also seen from Equation (3).
As per a zero inhibition affect shown by RNA-like ligands tested (Figure 3(A) and Figure 3(B)), their remarkable refolding capabilities   and [– O-----Mg2+] coordination input   are presumably beyond this phenomenon.
A clear pharmacological potential of oligo- and polydeoxyribinucleotides is a subject for numerous experimental and clinical studies performed since early 1990s      . Their applied medicinal significance, however, were treated predominantly by focusing on the aptomer properties, i.e. on capabilities to find the specific target molecules such as signaling proteins, membrane receptors, chromatin structure elements, etc      . Unlike our present work, therefore, these studies are all about the true docking participants. The inhibitory power of Poly(dNTP) species we found has nothing to do with their structures and composition being entirely dependent on molecular size (Figures 2(B)-(E), Figure 3(A), Figure 3(C), Figure 3(D), Figure 3(E)). This allows to “turn the page” in a long record of polynucleotide medicinal applications by just paying attention to the Poly(dNTP) motion on how to shut down a DNA repair in malignant cells. It makes sense for DNApolβ, key DNA repair enzymes, are found hyperexpressed in response to a high frequency of DNA damages followed by an increase of the cancer related cell proliferation rate      . With a respect to this statement, it has been already emphasized that the members of this enzyme family are the “legitimate targets” for cytostatic inhibitors like dNTP antimetabolites      and magnetic metal isotopes     .
There is a good enough understanding on molecular mechanisms beyond the inhibition of the cancer-hyperexpressed DNApolβ species provided by magnetic isotopes of bivalent metals—25Mg, 43Ca and 67Zn      . In particular, these mechanisms are dealing with the origin of “too short”, DNA repair insufficient, DNA fragments    . This effect leads to a massive release of the DNA repair related 40n - 100n DNA sequences with the unpredictable, unique structures   , i.e. this provokes a magnetic isotope induced formation of the DNApolβ endogenous inhibitors. It looks like a good explanation for cytostatic activity shown by magnetic metal isotopes in several cancer cells   .
Everything we know about pharmacokinetics of various DNA-based drugs and pharmacophores indicates to the fact that their bioavailability is far of being perfect mostly because of inevitable nucleases attack      . So this is the hardest task to manage a targeted delivery of Poly(dNTP) sequences to the DNApolβ-operating in situ compartments, for which some certain nanocarriers required     . As for the magnetic metal ions, they can be delivered to the DNApolβ in situ targets with   or even without   nanocationite administration which would make the magnetic isotope effect a promising tool to gain the DNA repair machinery breakdown in neoplasma.
Knowing that the abundance of 25Mg is relatively high (≈10%) and considering a remarkable role of magnesium in enzymatic phosphorylation processes    , it would be logical to suppose the existence of so called “hidden” effects of Magnesium-25 on numerous metabolic pathways. In this case, a high content of endogenous Fe2+ in cells and tissues of a living organism becomes a natural limiting factor to prohibit any expression of magnetic isotope effects in vivo. This is in accordance with the data on correlations between the 25Mg2+-affected ATP synthesis levels in mitochondria and the Fe2+ contents in these mitochondria isolated from different rat tissues  as well as with the results stated an increase of Fe/Mg ratios in several types of cancer (ovarian cancer, renal adenocarcinoma, fibroblast lung cancer, hepatocellular cancer, osteosarcoma, thyroid follicular adenocarcinoma) compared to corresponding normal, non-malignant, tissues     .
A variety of clinical case reports showing an appearance of short (100n - 300n) single-stranded DNA fragmets in a blood plasma of oncology patients   may now also be treated under a point of view of the probable DNA repair related origin of these tumor-released Poly(dNTP) sequences.
Last not least, the infamous quorum sensing phenomena  could be engaged with an effort to uncover a biological meaning of what we’ve found testing the capabilities of different Poly(dNTP) species to affect some tumor-specific DNA repair key enzymes.
Ultrashort (40n - 100n) polydeoxyribonucleotides are found to be the efficient non-specific inhibitors of DNA polymerases β from chromatin of several cancer cells: HL-60, WERI-1A, Y-79.
Manifesting a positive correlation between these inhibitory capabilities and the strength of affinity in enzyme-ligand pairs, such poly(dNTP) species promote a sharp suppression of enzymatic catalysis regardless on their primary structures. Only molecular size matters.
The data presented show a clear regulatory potential of some short ssDNA entities once they are about to interact with the key DNA repair enzymes.
This may provide a promising platform for further research aiming to shut down the DNA repair machinery in malignancies.
This work was performed within the aims and scope of the Russian Federal Specialized Program on priorities in science and technologies trends for 2014-2020 supported by Russian Federal Ministry of Science and University Education. The RF Government budget beyond.
ssDNA, Single-Stranded DNA;
DNApolβ, DNA Polymerase Beta;
MIE, Magnetic Isotope Effects;
AML, Acute Myeloid Leukemia.
 Buchachenko, A.L., Bukhvostov, A.A., Ermakov, K.V. and Kuznetsov, D.A. (2019) Nuclear Spin Selectivity in Enzymatic Catalysis. A Caution for Applied Biophysics. Archives of Biochemistry and Biophysics, 667, 30-35.
 Bukhvostov, A.A., Dvornikov, A.S., Ermakov, K.V., Kurapov, P.B. and Kyznetsov, D.A. (2017) Retinoblastoma: Magnetic Isotope Effects Might Make a Difference in the Current Anti-Cancer Research Strategy. Acta Medica (Hradec Kralove), 60, 93-96.
 Bukhvostov, A.A., Dvornikov, A.S., Ermakov, K.V. and Kuznetsov, D.A. (2017) Retinoblastoma Case: Shall We Get a Paramagnetic Trend in Chemotherapy? Archives of Cancer Research, 5, 158-162.
 Muller, W.E., Obermeyer, J. and Totsuka, A. (1974) Influence of Template Inactivators on the Binding of DNA Polymerases to DNA. Nucleic Acids Research, 1, 63-69.
 Corces, M.R., Granja, J.M., Shams, S., Louie, B.H., Seoane, J.A., Zhou, W., Silva, T.C. and Chang, H.V. (2018) The Chromatin Accessibility Landscape of Primary Human Cancers. Science, 362, 16-28.
 Ashley, J.S., Kronenberg, G.H., Lipman, K.R. and Bielka, H. (2019) Coupling the DNA Turnover Enzymes. Poly(dNMP) Ligands. In: Pitot, H. and Van Nijemen, J.T. Eds., Methods in Macromolecular Docking Research, University of Ghent Press, Ghent-Antwerp, 216-229.
 Bukhvostov, A.A., Shatalov, O.A., Orlov, A.P. and Kuznetsov, D.A. (2013) An Atypical DNA Polymerase Beta Overexpressed in Human AML/HL-60 Malignant Cells. Journal of Cancer Science and Therapy, 5, 94-99.
 Dewar, J.M. and Lyndall, D. (2012) Simple Non-Radioactive Measurement of Single-Stranded DNA. In: Bjergbaek, L., Ed., Methods in Molecular Biology, DNA Repair Protocols, Humana Press, Inc., Totowa, 920, 341-349.
 Fukami, T., Uchiyama, K. and Yoshimura, Y. (1996) Ultramicroanalysis by Use of Light-Scanning Photoacoustic Densitometry of Electrophoresed Protein. Analytical Biochemistry, 238, 60-67.
 Rastogi, C., Rube, H.T., Kribelbauer, J.F., Crocker, J., Locker, R.E., Martini, G.D. and Laptenko, O. (2018) Accurate and Sensitive Quantification of Protein-DNA Binding Affinity. PNAS, 115, E3692-E3701.
 Laurent, C., Neurath, K.J., Baglioni, G. and Sieliwanowicz, B. (2019) Advances in Multiwave UV-Spectrophotometry: RNP/DNP Integrity Studies. In: Lindsey, A.L. and Cohen, K., Eds., Physics of Biopolymers, Adler & Adler Publ., Perth, 41-56.
 Peterson, L.E. (2019) Small Molecule Docking of DNA Repair Proteins Associated with Cancer Survival Following PCNA Metagene Adjustment. A Potential Novel Class of Repair Inhibitors. Molecules, 24, 645-667.
 Wu, Y., Lu, J. and Kang, T. (2016) Human Single-Stranded DNA Binding Proteins: Guardians of Genome Stability. Acta Biochimica et Biophysica Sinica, 48, 671-677.
 Morten, M.J., Gamsjaejer, R., Cubeddu, L., Kariawasam, R., Peregrina, J., Penedo, J.C. and White, M.F. (2017) High Affinity RNA Binding by a Hyperthermophilic Single-Stranded DNA-Binding Protein. Extremophiles, 21, 369-379.
 Lyu, J., Wang, S., Balius, T.E., Singh, I., Levit, A., Moroz, Y.S. and O’Meara, M.J. (2019) Ultra-Large Library Docking for Discovering New Chemotypes. Nature, 566, 224-229.
 Zavyalova, E., Samoylenkova, N., Revishchin, A., Turashev, A., Gordeychuk, I., Golovin, A., Kopylov, A. and Pavlova, G. (2017) The Evaluation of Pharmacodynamics and Pharmacokinetics of Anti-Thrombin DNA Aptamer RA-36. Frontiers in Pharmacology, 8, 922-930.
 Squadrito, F., Bitto, A., Irrera, N., Pizzino, G., Pallio, G., Minutoli, L. and Altavilla, D. (2017) Pharmacological Activity and Clinical Use of PDRN (Polydeoxyribonucleotides). Frontiers in Pharmacology, 8, 224-233.
 Ashton, N.W., Bolderson, E., Cubeddu, L., O’Byrne, K.J. and Richard, D.J. (2013) Human Single-Stranded DNA Binding Proteins Are Essential for Maintaining Genomic Stability. BMC Molecular Biology, 14, 1-20.
 Ansari, A.S., Santerre, P.J. and Uludag, H. (2017) Biomaterials for Polynucleotide Delivery to Anchorage-Independent Cells. Journal of Materials Chemistry B, 5, 7238-7261.
 Svistunov, A.A., Napolov, Y.K., Bukhvostov, A.A., Shatalov, O.A., Alayutdin, R.N. and Kuznetsov, D.A. (2013) The Mitochondria Free Iron Content to Limit an Isotope Effect of 25Mg2+ in ATP Synthesis: A Caution. Cell Biochemistry and Biophysics, 66, 417-419.
 Mouliere, F., Chandrananda, D., Piskorz, A.M., Moore, E.K., Morris, J., Ahlborn, L.B. and Rosenfeld, N. (2018) Enhanced Detection of Circulating Tumor DNA by Fragment Size Analysis. Science Translational Medicine, 10, 117-129.
 Catachura, S.C., Leys, N. and Mastroleo, J. (2018) Quorum Sensing in Life Support Systems. In: Kalia, V.C., Ed., Quorum Sensing, Springer Nature, Ltd., Singapore, 249-260.