Tumors and biofilms: too much coincidences to be casual

The existence of the majority of microorganisms in the form of three-dimensional associates on the phase interface proves the significant survivable advantages of such form of life at compare with monocellular planktonic ones. These advantages provided to biofilms a place of the most widely distribu...

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Published in:Вiopolymers and Cell
Date:2018
Main Authors: Verevka, S.V., Voroshylova, N.M.
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Language:English
Published: Інститут молекулярної біології і генетики НАН України 2018
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Online Access:https://nasplib.isofts.kiev.ua/handle/123456789/154272
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Cite this:Tumors and biofilms: too much coincidences to be casual / S.V. Verevka, N.M. Voroshylova // Вiopolymers and Cell. — 2018. — Т. 34, № 1. — С. 72-81. — Бібліогр.: 35 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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author Verevka, S.V.
Voroshylova, N.M.
author_facet Verevka, S.V.
Voroshylova, N.M.
citation_txt Tumors and biofilms: too much coincidences to be casual / S.V. Verevka, N.M. Voroshylova // Вiopolymers and Cell. — 2018. — Т. 34, № 1. — С. 72-81. — Бібліогр.: 35 назв. — англ.
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container_title Вiopolymers and Cell
description The existence of the majority of microorganisms in the form of three-dimensional associates on the phase interface proves the significant survivable advantages of such form of life at compare with monocellular planktonic ones. These advantages provided to biofilms a place of the most widely distributed form of life if not the dominative one. There is a strong similarity in properties of biofilms and malignant tumors that promotes considering the latter as some kind of biofilms. Such point of view facilitates understanding some features of carcinogenesis as well as the grounds for perspective directions in the prevention of metastases. Існування більшості мікроорганізмів у формі тривимірних асоціатів на межі розподілу фаз свідчить про її значні переваги такої для виживання, порівняно з дисперсною формою, та дозволяє визначити біоплівки як домінуючу форму життя. Спостерігається виражена подібність багатьох властивостей біоплівок та злоякісних пухлин, що дозволяє провести певну аналогію між ними. Подібний погляд полегшує розуміння окремих рис карциногенеза та створює передумови для обґрунтування перспективних напрямків попередження метастазування. Существование большинства микроорганизмов в форме трехмерных ассоциатов на границе раздела фаз свидетельствует о значительных преимуществах для выживания по сравнению с дисперсным существованием, что позволяет определить биопленки как доминирующую форму жизни. Наблюдается выраженное подобие множества свойств биопленок и злокачественных опухолей, что позволяет провести определенную аналогию между ними. Подобный взгляд облегчает понимание отдельных черт карциногенеза и создает предпосылки для обоснования перспективных направлений предупреждения метастазирования.
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fulltext 72 S. V. Verevka, N. M. Voroshylova © 2018 S. V. Verevka et al.; Published by the Institute of Molecular Biology and Genetics, NAS of Ukraine on behalf of Bio- polymers and Cell. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited UDC 616-006:616-033-2:616-093/-098.001.8 Tumors and biofilms: too much coincidences to be casual S. V. Verevka, N. M. Voroshylova State institution “O. S. Kolomiychenko Institute of Otolaryngology Of National Academy of Medical Sciences of Ukraine” 3, Zoologichna, Kyiv, Ukraine, 02000 verevka.biochem@gmail.com The existence of the majority of microorganisms in the form of three-dimensional associates on the phase interface provides significant advantages as compared with unicellular plank- tonic ones. There is a strong similarity in properties of biofilms and malignant tumors that allows considering the latter ones as some kind of biofilms. Such point of view facilitates our understanding of some features of carcinogenesis and provides perspective directions in the prevention of metastases. K e y w o r d s: biofilms, carcinogenesis, metastasis The most widely distributed form of life Arthur Kornberg noted once, that multicellular organisms, including mammals, are the rare exclusion in the world that belongs to micro- organisms [1]. Up to 95–99% of them exist in natural environments in the form of bio- films [2]. In other words, biofilms represent the most widely distributed and successful model of life on the Earth [2]. According to the universally acknowledged definition, they are aggregates of microorganisms in which cells are frequently embedded in a self-pro- duced matrix of extracellular polymeric sub- stances that are adherent to each other and/or surface [3]. All higher organisms, including humans, are colonized by microorganisms that form biofilms, which can be associated with persistent infections in plants and animals, and with contamination of medical devices and implants [5]. What are the advantages of as- sociated form of microorganisms’ life in con- trary to quite rare free planktonic one? These advantages have to be extremely significant because they determine the choice of biofilm’s form of life by immeasurable diversity of mi- croorganisms. Unfortunately, the same advan- tages were suitable for multicellular organisms with the grave consequences for the latter. The importance of being biofilm Biofilms are complex systems that have high cell density, ranging from 108 to 1011 cells g-1 Discussions ISSN 1993-6842 (on-line); ISSN 0233-7657 (print) Biopolymers and Cell. 2018. Vol. 34. N 1. P 72–81 doi: http://dx.doi.org/10.7124/bc.000972 73 Tumors and biofilms: too much coincidences to be casual wet weight, and typically comprise many spe- cies. As a rule, biofilms are formed in flow system in the presence of the necessary growth substrates. A further source of heterogeneity is the ability of cells to undergo differentiation, which can be triggered by local conditions, and to coordinate life cycles that include stage- specific expression of genes and proteins. That is typical for the growth and development of microorganisms in spatially heterogeneous systems. The emergent properties of biofilm communities comprise novel structures, ac- tivities, patterns and properties that arise dur- ing their growth that leads to the formation of self-organized complex system [4]. There is an opinion that the key condition for the bio- films formation is the presence of some factor which suppresses significantly the growth of individual microorganisms [5]. This point of view has the right to exist, although often in the absence of adverse factors microorganisms are still inclined to form biofilms. The list of hostile factors seems to be endless and con- tains innumerous chemical toxicants, antibiot- ics, oxygen reactive species, metal ions, ionic force, temperature, pH, detergents and desic- cation. The list of has to be supplemented by more complicated defensive systems when we consider microorganisms living inside multi- cellular organisms. All these factors suppress the development of separate microorganisms and lead to the formation of biofilms. There are a lot of processes both at molecular and cellular levels that promote the intercellular association. Thus, the influence of an unfavor- able factor alters the normal metabolism of microorganisms. This leads to the production of significant number of abnormal proteins, lipids, and carbohydrates that may be evalu- ated as some kind of endogenous intoxication at the simplest, unicellular level [6]. It is known that proteins with imbalanced or in- complete structures interact with outer cell membranes by quite rigid rules, which leads to the anchoring of hydrophobic residues in- side membrane where as the positively charged ones were directed inside the cell (“positive- inside” rule [7]). Such allocation creates even ideal conditions for non-enzymatic glycosyl- ation, or rather for interaction of intracellular part of the protein with numerous carbonyl- containing compounds, whose content in the cell increases sharply when cell is exposed to unfavorable factors. At the same time glycation of the protein intracellular part creates precon- ditions for exposure of bulky and chemically active carbohydrate derivatives on the cell surface. The following growth of extracellular cover may pass by well-known mechanisms of advanced glycation end products (AGEs) self-assembling with the formation of numer- ous intermolecular and intercellular bounds. In addition, non-functional glycation is a well- recognized inducer of the conformational rear- rangement of the protein molecules into β-fold structures that are capable of self-assembly into amyloid-like fibrils [8, 9]. Formation of such mixed cover on the outer cell membrane protects to some extent the cell from the con- tact with hostile environment and persists at mitotic division to both newly formed cells. These and similar associative processes sup- port the mutual adhesion of dividing cells and the formation of an extracellular polymeric substance (EPS). Evidently the given examples are far from the exhausting of the set of the processes that lead to the formation of three- dimensional cells’ coat, but even they are 74 S. V. Verevka, N. M. Voroshylova enough for the transformation into autoch- tonic parametabolic process that outruns cells division. At such look the community of free- born microbes may be recognized as the mise- rable lump of the clayed poor fellows, that by the skin of their teeth survive in the hostile habitat. However, EPS isn’t a simply amor- phous gel that is composed by polysaccharides, lipopolysaccharides, and glycoproteins, but instead has a highly ordered three-dimension- al structure that contributes to its function and emergent properties [10–12]. It provides the protection of microorganisms, redistribution of nutrients between individual cell layers and accumulation of active intracellular compo- nents in inaccessible for free microorganisms concentrations. EPS accumulates inside the matrix innumerous substances that may be inactivated or transformed into nutrients by various enzymes, that were secreted by cells and immobilized in EPS’ net. All these proper- ties transform the EPS matrix in some kind of external digestion system [13]. Survivorship bias at microbial level There is no consensus on the causes of phe- notypic variation of microorganisms at the biofilm forming. Some components of the extracellular polymeric substances may be mutagenic. The horizontal gene transfer may be also possible due to enriching the genome of compactly grouped microorganisms by various inclusions of extracellular DNA [4, 5]. The exchange on genetic information may play a notable role in the intercellular interac- tions in biofilm, but in clean and feed-abun- dant conditions such enrichments are at best useless and mutant forms lose to normal one, lag behind in the dynamics of reproduction and eventually disappear. Contrary, under the influence of an unfavorable factor, some (the rarest) change in the genome prove to be use- ful, ensuring to mutant form advantages in surviving and multiplication over an original form. It is impossible to exclude the possibi- lity of evolutionarily formed permanent phe- notype dispersion with an unchanged geno- type. Pheno ty pic plasticity seems to be the most important prerequisite for survival. The community of the cells that are phenotypi- cally different among themselves proves to be more adapted to survival and reproduction under the influence of any unfavorable factor. The plasticity of the phenotype is also neces- sary for the formation of internal layers of biofilm under conditions that differ from both an ideal pure medium and conditions of hab- itation of the outer layers of the forming film. Thus, at certain thickness of the outer layer the transition from aerobic metabolism to anaerobic one becomes in demand. No less useful are the abilities to supply catabolites of the outer la yers’ cells, extracellular poly- meric substance, died or less aggressive cells, and even the material of the supporting sur- face [4, 14]. Biofilms’ habitat conditions pre- determine an increase of aggressiveness and intensive production of lytic enzymes. The expansion of new food base supports the domination of the fittest iso-forms. Less suc- cessful cells as well as that ones which got under annoying conditions, are eliminated by more luckier relatives and bacteriopha- ges [15]. In this way, spontaneously but reg- ularly, feeding cavities, chanels, and pores are forming. Deepening the cells’ differentiation by the biofilm development leads to the formation of 75 Tumors and biofilms: too much coincidences to be casual subpopulations with properties that are very different from the free form of the same cells. As a result, the concept has emerged of the special “biofilm phenotype”, which in com- munity is less sensitive for the influence of the corresponding unfavorable factors [4, 16]. There is no doubt that the formation of “win- ning” lines is not a single act of creation, but proceeds permanently, with a constant rejec- tion of less adapted forms. Therefore, the con- sideration of the formation of biofilms as a purposeful process is a typical example of a systematic survivorship bias – accounting for winning cases without considering the many losers. Of the many phenotypic forms that are formed, only those ones whose phenotype contributes to survival and reproduction under the yoke of an unfavorable factor or changed environmental conditions are observable. Both the initial planktonic form, and innumerous ones with useless or harmful changes of phe- notype, lose in distribution and, as a result, lose in representation. But this doesn’t mean that they are still not forming. From this point of view the systematically formed failure forms are an indispensable condition for the adaptation and survival of society as a whole. There is nothing unusual in this, if notify that microbes are the product of the selection du- ring the myriad generations. The formation of the aggregate isn’t a consequence of the sti- cking together of individual cells, but is the result of proliferation of the cellular forms which were more adapted to the given condi- tions. On these reasons biofilms are neither “fortresses” nor “cities”, but they are the result of rigid selection of cells by phenotype con- formity or inconsistency for the changed ha- bi tat conditions. Under the pressure of the immune system For obvious reasons, the features of biofilms’ existence inside the higher organisms are of increased interest. The main feature of this coexistence is the presence of powerful pro- tective systems designed to neutralize or re- move the alien inclusions from the body. In this case, the recognition of «one’s own» and «others» is determined by the presence or absence on the cells’ surface of structural groups that don’t conform to the structural rules adopted in this particular biological system [17]. One can confidently identify three key strategies for the survival of micro- organisms under similar circumstances. The simplest and most successful one is based on the reaching of the maximal correspondence of the cell’s surface to the structural rules adopted by multicellular proprietary organ- ism. This strategy is the typical one for most obligate microorganisms that live in biofilms whose outer layer doesn’t cause noticeable reaction of the host’s defensive systems. A more complex case is represented by micro- organisms that change antigenic determinants of the surface after the forming of a full-scale immune response to them. Such strategy is quite videspread among various bacterias and protosoas, which in contrast to Leopard may change their spots. For example, an African trypanosomias (Trypanosoma brucel) makes such transformations up to 20 times, that fi- nally leads to the death of the host [18]. In such cases the decisive demands are the phe- notypic plasticity and rigid selection of forms that were acceptable for changing environ- mental conditions. In some cases microorgan- isms may minimize the impact of immune 76 S. V. Verevka, N. M. Voroshylova system by formation of a kind of smoke bar- ragen by intensive biosynthesis of the sub- stances, which interaction with environmen- tal components leads to the formation of im- munogenic compounds with corresponding redistribution of the immune system’s action. All the noted strategies do not contradict to each other and may be used together. So, Strepto coccus pyogenes and Staphylococcus aureus are typical obligate microorganisms existing in the form of biofilms. They do not create any problems for the carrier at the normal functioning of the immune system. However, both of them produce intensively the proteins, that initiate activative processes resulting in the formation of significant amounts of immunogenic derivatives. Thus, streptokinase produced by Streptococcus pyo- genes forms a complex with plasminogen circulating in the bloodstream. Such a com- plex, in turn, activates other molecules of plasminogen to free plasmin that is immedi- ately blocked by α2-an ti plasmin. The plasmin- α2-antiplasmin complex is recognized by clearance systems as a protein to be elimi- nated immediately [19]. Staphylo co ccus au- reus produces staphylokinase that acts simi- larly, even in some simplified manner. Both proteins possess little immunogenicity and are not needed for their cells-producers in itself, but derivatives of these proteins redis- tribute substantially the influence of immune system from producer cells. That leads to the survival of the latter in a state of quasi-sta- tionary equilibrium with the host organism. Meanwhile, the weakening of immune system caused by any reasons reduces the restrictions of microorganisms’ growth, that leads to the hard consequences. … let slip the dogs … Mutual negative interactions of the familiar cells have also been observed in biofilms. Competition between cells inside biofilms can involve various killing mechanisms, such as those using antibiotics, bacteriocins, or extra- cellular membrane vesicles (which can contain enzymes that kill or impede the growth of competiting organisms), or strategies that com- promise growth, such as nutrient depletion or the inhibition of quorum sensing [4, 20]. Thus, the binary biofilm is formed by two Rumi no- so ccus species, one of which forms a bacterio- cin active against the other [21]. For the same reasons biofilms release significant amount of substances that inhibit the growth and repro- duction of free planktonic forms as well as those ones which were pulled out by the bio- film on the late stage of maturation. These substances play the role of some kind of self- produced adverse factor. That is why the pos- sibilities of free cells’ spreading with following forming new biofilms are determined by the complex of external unfavorable factors, by the ability of plankton forms for mutual bind- ing, and by the availability of a substrate suit- able for the primary sorption. No less signifi- cant is the ability of these microorganisms to retain certain phenotypic acquisitions irrespec- tive of the initial conditions. That is why some phenotypes become even impossible to self- propagation in the absence of hostile factor and are doomed to disappear. On the contrary, some other biofilm-origin microorganisms sur- vive at returning to a free planktonic state, or rather, when dividing cells pass through this stage. That is the cause of the endless race between the spread of diseases which infec- tious agents became resistant to some antibio- 77 Tumors and biofilms: too much coincidences to be casual tics and the development of qualitatively new drugs, for which the resistance has not been formed yet. In some cases the weakening of the master’s organism counteraction leads to the spread of biofilm formed cellular iso-forms with increased aggressiveness and altered nu- trient speci fi ci ty. Therefore, the transformation of known obligate microorganisms at the weakening of the immune system into the hard damaging factor is natural and inevitable. Together with the previously developed resis- tance to antibiotics, this transformation can be lethal for the host. Too much coincidences to be casual The concept of biofilms has been proposed recently – in the mid-1980s [22]. It is wide- spread mainly among microbiologists, infec- tious disease specialists, biotechnologists and ecologists, whereas for the numerous repre- sentatives of other branches of biological and medical sciences it remains as a kind of exo tics that is very far from their interests. However, even the simplest comparison of the regulari- ties of formation and development of biofilms and malignant tumors is striking by similarity. In both cases we are dealing with the formation of three-dimensional associates of cells, which differ sharply from the environment. Whatever the reasons for the formation of malignant cells, a metabolic disorder is accompanied by a massive contamination of the outer cell membrane by the binding of the diverse extra- cellular material. This, on one hand, causes a regular reaction of the immune system, that may be considered as the powerful unfavorable factor that promotes the formation of the bio- film. On the other hand, high reactivity of the surface carbohydrate components provides both mutual recognition of tumor cells and endotheliocytes’ surface, ensuring primary adhesion of tumor cells to the endothelium of the vessels of the target organ that is the key stage of metastasis [23, 24]. At the same time, the material adsorbed on the cell surface initi- ates a cascade of activative processes, that lead to the cleavage of surrounding tissues, the development of oxidative stress and other pro- cesses resulting in the formation of significant amounts of various abnormal metabolites [25]. Some of them, forming and accumulating in the tumor tissue in concentrations which are unattainable for a single cell, cause an unpre- dictable cascades of cells’ transformations with a rigid selection of formed cellular isoforms according to the criteria considered above for the biofilms. Other components contribute to the tumor survival by damaging surrounding tissues and reducing the impact of the immune system by smoke screen of damaged proteins. The intercellular stroma of the tumor is a typ- ical extracellular polymeric substance by both: its content and functions [26]. The presence of β-structured protein aggregates in stroma’s composition is also understandable and is similar for the cases of biofilms and for some other tissues with disturbed metabolism [7]. It is worth to underline, that the formation of β-stacked protein aggregates in the living body in itself leads to severe consequences associ- ated with the disruption of the normal func- tioning of a number of biological systems. A special group of tumor-producing substan ces are the tumors’ restrictors, that more or less effectively block the interactions essential for metastasis and invasion [27, 28]. Similarly to biofilms, the reaching of the three-dimension- al tumor’s size causes the cells’ differentiation, 78 S. V. Verevka, N. M. Voroshylova formation of feeding vessels and changes in the character and intensity of the local me- tabolism. Thus, the increase in growth factors expression is the typical tumors feature and may be caused by phenotypic differentiation. At the same time the development of nonfunc- tional proteolysis, which is typical for malig- nant processes, leads to the activation of growth factors followed by intensification of angiogenesis, which is typical for tumor de- velopment, too [29]. All these alterations are not a directional process, but are the result of a complex of processes leading to the forma- tion of phenotype-different forms with subse- quent selection according to the criterion of the ability to survive and divide under perma- nently changing conditions. The marked analogy of the processes of formation of biofilms and malignant neoplasms makes it possible to draw several conclusions that can have practical significance. If to ex- amine tumor as a kind of a mature biofilm, the high phenotypic plasticity of the tumors’ cel- lular society complicates significantly, if not excludes completely, the blocking of the ma- lignant process by the body itself. The same reasons cause the formation of chemotherapy- resistant forms similarly to the formation of antibiotic-resistant biofilms. Thus, the forma- tion of cytostatics-resistant tumor cells is caused by a change in the lipid composition of their outer membranes, leading to decrease in permeability for cis-platin and doxorubi- cin [30, 31]. At the same time, resistance to liposomal forms of these cytostatics has not been detected, which clearly indicates the ad- visability of using preparations with enhanced membrane permeability in the treatment of recurrent oncological diseases [31, 32]. The process of metastasis is mediated by the stage of formation of a “floating island” of malignant cells [23]. By the analogy with the mechanisms of formation and development of biofilms, it it is possible to suppose that in this state the conglomerate of malignant cells is the most vulnerable. It is known that only a small part of malignant cells circulating in the blood- stream is capable of anchoring with the sub- sequent formation of a tumor. In other words, the limiting stage of the metastasis is the bind- ing of floating cells to suitable landing sites on the intima of blood vessels. Similarly to the biofilm-forming processes, this process is li- mi ted by a number of tumor-produced sub- stances that block the binding sites and boun- ded groups, which are responsible for cells’ sorption. The elimination of tumor removes these blocking compounds, thus creating the prerequisites for relapse. This necessitates the postoperative use of angiostatins, trombospon- dins and similar substances for limitation of undesirable sorptive processes. An important consequence of the formation of antimetasta- tic-resistance is the increase in the aggressive- ness of cells, which is associated with activity of the proteolytic enzymes. Thus, for cytos ta- tics-resistant cells more than triple increase in trypsin-like activity was shown [33]. By ana- lo gy with the mechanisms of biofilm develop- ment, such increase in aggressiveness is a di- rect consequence of the selection of more ag- gressive cellular isoforms, which are more adapted for surviving under the pressure of more complicated complex of unfavorable factors. It is worth to emphasize that proteo- lytic enzymes formed due to non-functional activation are structurally damaged and can’t be blocked by the protein inhibitors of blood 79 Tumors and biofilms: too much coincidences to be casual circulation. This encourages the search for biocompatible inhibitors of proteinases, that are different in the mechanism of action from ineffective natural ones. For these reasons the experimental work on the suppression of recur- rence by protein inhibitors of thrombin from the leech salivary glands deserve attention [34, 35]. It seems that such drugs may not only effectively prevent the development of post- operative thromboses, but also have significant antimetastatic effects. Conclusions The presented data testify for a possible simi- larity of the processes of the formation of biofilms and malignant tumors. It also follows that the formation of multicellular anomalies is largely mediated by the action of a complex of non-enzymatic processes. The components of this complex of reactions proceed autoch- thonically and independently, but their total action ensures the survival of more adapted cellular forms. Such an order is disastrous for less adapted cells, but it ensures the survival of society as a whole. In both cases, the forma- tion and development of a multicellular as- sociate is a consequence of a complex of bio- chemical and biophysical processes, that lead to the permanent formation of phenotypically different forms with permanent selection ac- cording to the changing environment, which is permanent, too. In the mature state both biofilms and tumors have increased resistance to a variety of unfavorable factors. Therefore, the suppression of undesirable processes is more effective at the early stages of their de- velopment that leads to the search for ways to influence on the less resistant early forms. Both biofilms and tumors produce substances that limit the spread of the free forms of corre- sponding cells. That is why the usage of these substances is necessary after tumor elimina- tion. At the same time free cells’ forms are more vulnerable for the substances, that are able to limit their aggressivity. 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Biol Pharm Bull. 2008;31(4):696–702. 35. Lu Q, Lv M, Xu E, Shao F, Feng Y, Yang J, Shi L. Recombinant hirudin suppresses the viability, adhe- sion, migration and invasion of Hep-2 human laryn- geal cancer cells. Oncol Rep. 2015;33(3):1358-64. Пухлина та біоплівки: забагато співпадань, щоб бути випадковими С. В. Верьовка, Н.М. Ворошилова Існування більшості мікроорганізмів у формі тривимір- них асоціатів на межі розподілу фаз свідчить про її зна- чні переваги такої для виживання, порівняно з дисперс- ною формою, та дозволяє визначити біоплівки як до- мінуючу форму життя. Спостерігається виражена поді- бність багатьох властивостей біоплівок та злоякісних пухлин, що дозволяє провести певну аналогію між ними. Подібний погляд полегшує розуміння окремих рис кар- циногенеза та створює передумови для обґрунтування перспективних напрямків попередження метастазування. К л юч ов і с л ов а: біоплівки, карциногенез, мета- стазирование. Опухоль и биопленки: слишком много совпадений, чтобы быть случайными С. В. Веревка, Н. М. Ворошилова Существование большинства микроорганизмов в фор- ме трехмерных ассоциатов на границе раздела фаз свидетельствует о значительных преимуществах для выживания по сравнению с дисперсным существова- нием, что позволяет определить биопленки как доми- нирующую форму жизни. Наблюдается выраженное подобие множества свойств биопленок и злокачествен- ных опухолей, что позволяет провести определенную аналогию между ними. Подобный взгляд облегчает понимание отдельных черт карциногенеза и создает предпосылки для обоснования перспективных направ- лений предупреждения метастазирования. К л юч е в ы е с л ов а: биопленки, карциногенез, метастазирование. Received 23.05.2017
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institution Digital Library of Periodicals of National Academy of Sciences of Ukraine
issn 0233-7657
language English
last_indexed 2025-12-07T17:23:58Z
publishDate 2018
publisher Інститут молекулярної біології і генетики НАН України
record_format dspace
spelling Verevka, S.V.
Voroshylova, N.M.
2019-06-15T12:11:48Z
2019-06-15T12:11:48Z
2018
Tumors and biofilms: too much coincidences to be casual / S.V. Verevka, N.M. Voroshylova // Вiopolymers and Cell. — 2018. — Т. 34, № 1. — С. 72-81. — Бібліогр.: 35 назв. — англ.
0233-7657
DOI: http://dx.doi.org/10.7124/bc.000972
https://nasplib.isofts.kiev.ua/handle/123456789/154272
616-006:616-033-2:616-093/-098.001.8
The existence of the majority of microorganisms in the form of three-dimensional associates on the phase interface proves the significant survivable advantages of such form of life at compare with monocellular planktonic ones. These advantages provided to biofilms a place of the most widely distributed form of life if not the dominative one. There is a strong similarity in properties of biofilms and malignant tumors that promotes considering the latter as some kind of biofilms. Such point of view facilitates understanding some features of carcinogenesis as well as the grounds for perspective directions in the prevention of metastases.
Існування більшості мікроорганізмів у формі тривимірних асоціатів на межі розподілу фаз свідчить про її значні переваги такої для виживання, порівняно з дисперсною формою, та дозволяє визначити біоплівки як домінуючу форму життя. Спостерігається виражена подібність багатьох властивостей біоплівок та злоякісних пухлин, що дозволяє провести певну аналогію між ними. Подібний погляд полегшує розуміння окремих рис карциногенеза та створює передумови для обґрунтування перспективних напрямків попередження метастазування.
Существование большинства микроорганизмов в форме трехмерных ассоциатов на границе раздела фаз свидетельствует о значительных преимуществах для выживания по сравнению с дисперсным существованием, что позволяет определить биопленки как доминирующую форму жизни. Наблюдается выраженное подобие множества свойств биопленок и злокачественных опухолей, что позволяет провести определенную аналогию между ними. Подобный взгляд облегчает понимание отдельных черт карциногенеза и создает предпосылки для обоснования перспективных направлений предупреждения метастазирования.
en
Інститут молекулярної біології і генетики НАН України
Вiopolymers and Cell
Discussions
Tumors and biofilms: too much coincidences to be casual
Пухлина та біоплівки: забагато співпадань, щоб бути випадковими
Опухоль и биопленки: слишком много совпадений, чтобы быть случайными
Article
published earlier
spellingShingle Tumors and biofilms: too much coincidences to be casual
Verevka, S.V.
Voroshylova, N.M.
Discussions
title Tumors and biofilms: too much coincidences to be casual
title_alt Пухлина та біоплівки: забагато співпадань, щоб бути випадковими
Опухоль и биопленки: слишком много совпадений, чтобы быть случайными
title_full Tumors and biofilms: too much coincidences to be casual
title_fullStr Tumors and biofilms: too much coincidences to be casual
title_full_unstemmed Tumors and biofilms: too much coincidences to be casual
title_short Tumors and biofilms: too much coincidences to be casual
title_sort tumors and biofilms: too much coincidences to be casual
topic Discussions
topic_facet Discussions
url https://nasplib.isofts.kiev.ua/handle/123456789/154272
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