Analysis of abnormal intestinal flora on risk of intestinal cancer and effect of heparin on formation of bacterial biofilm.

To study the effect of abnormal intestinal flora on the risk of colorectal cancer and the effect of heparin on the formation of bacterial biofilm, 50 patients with colorectal cancer and 50 healthy subjects were selected. The distribution and quantity of bacteria in feces, the levels of D-lactic acid and endotoxin in serum of the two groups were detected. Intestinal flora strains and biofilm growth were also detected in patients with colorectal cancer cultured in different heparin concentrations (0 mg/mL, 5 mg /mL, 10 mg/mL, and 20 mg/mL). The results showed that there was significant difference in the number of major strains of intestinal flora between healthy subjects and colorectal cancer patients before and after operation (P < 0.05). The serum D-lactic acid levels (1.41 ± 0.39, 6.38 ± 1.42 μg/mL) and endotoxin levels (0.62 ± 0.09, 0.80 ± 0.15 EU/mL) in the experimental group were higher than those in the control group (0.91 ± 0.52 μg/mL) (0.05 ± 0.02 EU/mL) before and after operation (P < 0.05). The amount of biofilm formation increased significantly with the increase of heparin concentration (P < 0.05). In summary, there was a close relationship between the occurrence of colorectal cancer and abnormal intestinal flora. Heparin may have a positive effect on regulating intestinal flora in patients with colorectal cancer, which provided certain reference value for the treatment of colorectal cancer.

Introduction

The incidence of intestinal cancer has increased year by year in humans around the world. The pathogenesis of intestinal cancer may be closely related to human eating habits, lack of exercise, body obesity, and other lifestyles. The susceptibility and development of this type of disease are inseparable from the joint effect of the genetic environment. Most of the precancerous mechanisms of intestinal cancer have been researched and developed [1]. Cellular and molecular biological mechanisms of abnormal crypt-adenoma-intestinal cancer intestinal cancer have been extensively studied by colleagues all over the world. Nevertheless, the role of environmental factors in the development of such diseases as intestinal cancer is still not completely clear clinically for humans. Molecular biology technology has been developed and widely used with the progress of human society, and there are National Institutes of Health (NIH) Human Microbiome Project (HMP). In addition, the EU metagenomics of the human intestinal tract (Meta HIT) was launched in 2008. As a result, human beings have gradually begun to pay attention to the intestinal flora as an important environmental factor in the occurrence and development of various intestinal cancers, which have an extremely important position and role [2,3].

Current studies believed that the types and quantities of intestinal flora are closely related to human diet, living habits, geographical environment, age, and health conditions [4,5]. It has been reported that the composition of gut bacteria changes with age, for example, newborn babies have the same flora in all parts of their bodies. However, the structure of intestinal microflora of infants gradually transformed to that of adults after their dietary habits were close to that of adults. Human intestinal microbiota is relatively stable in adulthood, and facultative anaerobic bacteria increase in the intestinal microbiota in old age, while the immune system function begins to decline [6]. When the balance of intestinal flora is broken, probiotics will passively transform into pathogenic bacteria through gene transfer, resulting in a decrease in the number of probiotics. The pathogenic bacteria take the opportunity to multiply, further destroy the balance of intestinal flora, causing bacterial imbalance. In another way, intestinal bacteria and their products, lipopolysaccharide (LPS, a chemical component unique in the outer wall of Gram-negative bacteria), are transferred to tissues and organs outside the intestinal tract or even to blood through the intestinal mucosal barrier, further causing intestinal microbiome disorder [7]. When trauma, massive bleeding, cardiogenic, or septic shock occurs, the body redistributes blood to protect the heart, brain, and other important organs. Intestinal mucosa and submucosa blood flow decreased, and mucosal epithelial cell necrosis appears, creating favorable conditions for bacterial migration. At this time, pathogenic bacteria in the intestinal tract transfer, resulting in disruption of intestinal balance, and even more, pathogenic bacteria that should be in the intestinal tract further multiply after displacement [8-10].

Heparin has been used worldwide as a clinical anticoagulant for nearly 100 years since its discovery. However, due to the difficulty of purification and complicated synthetic methods of heparin, the research on heparin is not common. Heparin is a highly sulfated glycosaminoglycan with uneven chain length. Although it has been reported that heparin promotes bacterial biofilm formation, the relationship between heparin structure and bacterial biofilm formation remains unclear. Some studies suggested that heparin stimulates the formation of bacterial biofilm in a dose-dependent manner. Both the sulfonic groups and molecular weight of heparin molecules contribute to enhancing the formation of bacterial biofilms [11]. The S/N ratio of low molecular weight heparin is slightly increased by depolymerization of heparin under acidic conditions. In this study, it was found that adding low-molecular-weight heparin to the culture medium did not significantly stimulate bacterial biofilm formation. However, whether heparin can significantly stimulate the formation of bacterial biofilm has not been explained. In addition, the formation of S. Typhimurium biofilm was studied by adding heparin derivatives, and the results of the above studies were consistent [12]. Moreover, there are few studies on the relationship between the biofilm formed under the influence of heparin and intestinal flora. Therefore, it was hoped to study the intestinal flora of patients with colorectal cancer and its correlation with the risk of colorectal cancer. On this basis, this study also innovatively carried out the verification experiment of heparin on the biofilm image of bacterial community, hoping to provide some reference value for the study of intestinal microbiome-related mechanism of colorectal cancer disease.

Materials and methods

Research object and materials

In this study, 50 patients who received surgical treatment for intestinal cancer in our hospital from January 2020 to January 2021 were selected, including 28 males and 22 females. In addition, 50 healthy subjects who underwent physical examination in the physical examination center of the same hospital were selected as the control group, including 27 males and 23 females. This study was approved by the Medical Ethics Committee, and the patient and their families understood the content and method of the study and agreed to sign the appropriate informed consent form.

Kit instruments used in this study included heparin sodium (Shandong Zaozhuang Sanokang Biochemical Co., LTD.), Petri dish (Taixing Likang Medical Instrument Co., LTD.), and culture medium, inoculation ring, and serum detection kit (purchased from Beijing Yanda Biotechnology Co., LTD.).

Inclusion and exclusion criteria

The clinical diagnosis of intestinal cancer was confirmed according to the patient’s clinical symptoms, signs, colonoscopy, tumor markers, and the results of tissue biopsy. Patients with acute abdomen such as acute intestinal obstruction and intestinal perforation were excluded. Patients with poor general conditions such as severe malnutrition and cachexia also were excluded and not included in the experimental group. Patients with other serious diseases such as liver and kidney failure, immune deficiency, etc., and patients who had recently used antibiotics, microecological agents, and was with acute infectious diseases that may affect the distribution of intestinal flora were excluded from the experimental group.

Methods

In this study, the intestinal microbiota of the subjects was studied by analyzing the microbial composition and the proportion of each component in their feces. The following were the detection and identification methods of feces microorganisms of subjects adopted in this study [13].

First, fresh stool samples were collected from 100 subjects, and it was ensured that they were sent for testing within 30 minutes. In the bowel cancer group, stool collection time was three days before surgery and the first natural defecation after surgery. After that, 0.1 g stool and 0.9 mL 0.9% sodium chloride injection were extracted from the collected stool samples and added into the EP tube, and the mixture was diluted for multiple times. Then, 0.05 mL of fecal solution with different diluted concentrations were absorbed and inoculated on selective medium plates. During the culture process, the culture temperature was 37°C, and the culture lasted for 18 h-24 h. After that, the distribution, number and types of bacteria in the culture medium were observed by microscope. Finally, a counting plate was used to record the approximate number of bacteria in the bacterial population, so as to determine the composition and proportion of the intestinal flora of the subjects. The number of colonies (Log10) grams of live bacteria in feces was calculated according to Equation (1).

To identify bacterial species, the purity, colony morphology, and Gram staining results of the bacteria in the smear were observed first. Then, 3 ml of inoculum was used to prepare the bacterial strain into a suspension equivalent to Mc-Farland3-Mc-Farland5 standard solution, and 50 μl of suspension was added into the substrate-containing well and two control wells of the identification plate. After incubation with the drug sensitivity analysis system for microbial identification, the bacterial identification results were recorded. A part of fecal bacterial liquid from healthy people in the control group was retained to exclude the error caused by the effect of bacterial liquid from intestinal cancer patients on the experimental results, and used to determine the effect of heparin on it.

Bacterial growth curve determination

The fecal bacteria liquid of healthy subjects was prepared by referring to the method in Section 2.3, and then the fecal bacteria liquid of healthy subjects was detected by ultraviolet spectrophotometry [14], and its maximum absorption peak was D600.

In addition, fecal bacteria from healthy subjects and colorectal cancer patients were transferred to 20 mL M9C medium containing different concentrations of heparin. Three parallel experiments were set for the concentration of heparin in each group, and the concentration gradients of heparin used in the experiments were 0 mg/mL, 5 mg/mL, 10 mg/mL, and 20 mg/mL, respectively. The inoculated petri dishes were placed in a shaking table for 37°C shaking culture. The shaker was taken out from the shaker at regular intervals, and the OD600 of bacterial liquid was detected by spectrophotometer and recorded until 12 h.

Serum D-lactic acid and endotoxin detection

Peripheral venous blood was collected from colorectal cancer patients and control subjects before serum D-lactic acid and endotoxin detection. After serum was isolated from venous blood, the relative contents of d-lactic acid and endotoxin in serum of the samples were detected by ELISA [15]. The blood collection time of the intestinal cancer group was 3 days before operation and 24 hours after operation. The detection methods and steps were carried out in strict accordance with the kit instructions.

Statistical methods

Statistical analysis was performed using SPSS 17.0. The measurement data were expressed by mean plus or minus standard deviation (±s), and the comparison between groups was performed by t test. The comparison of count data was conducted by chi-square test. P < 0.05 indicated that the difference was statistically significant.

Results

In this study, the intestinal flora of patients with colorectal cancer and its correlation with the risk of colorectal cancer were studied. An innovative experiment was conducted to verify the effect of heparin on microbial biofilm, hoping to provide some reference value for the study of intestinal microbiome-related mechanism of colorectal cancer disease. By comparing the gut microbiota of patients with colorectal cancer with that of healthy subjects, the influence of abnormal intestinal flora on the risk of colorectal cancer was discussed. The influence of heparin on the formation of microbial biofilm was investigated by studying the growth of microbial biofilm under different heparin concentration gradients. The major results of this study were as follows.

Comparison of basic information

Figure 1 was the basic information graph of the research object. There was no significant difference in average age and sex ratio between the experimental group and the control group (P > 0.05).

Figure 1.

Basic information of the research object.

Patient’s intestinal flora distribution

Figure 2 shows the comparison of microflora distribution between colorectal cancer patients and healthy people before surgery. The number of live colonies of Escherichia coli, Enterococcus faecium, Campylobacter, Bifidobacterium, and Lactobacillus before surgery in colorectal cancer group were (7.69 ± 1.61) Log10, (6.89 ± 1.71) Log10, (7.42 ± 1.53) Log10, (7.39 ± 0.93) Log10, (7.41 ± 1.28) Log10, respectively. Compared with healthy control group, the number of viable colonies of Escherichia coli and Enterococcus faecalis increased significantly. The number of living colonies of Campylobacter, Bifidobacterium, and Lactobacillus decreased significantly, with statistical significance (P < 0.05).

Figure 2.

Comparison of flora distribution between intestinal cancer patients before surgery and healthy controls.

Figure 3 shows the comparison of bacterial community distribution between patients with colorectal cancer and healthy people after surgery. The number of viable colonies of Escherichia coli, Enterococcus faecalis, Campylobacter, Bifidobacterium, and Lactobacillus after operation in colorectal cancer group was (8.72 ± 1.71) Log10, (8.01 ± 1.83) Log10, (6.13 ± 1.49) Log10, (5.99 ± 0.98) Log10, and (6.17 ± 1.31) Log10, respectively. Compared with healthy control group, the number of viable colonies of Escherichia coli and Enterococcus faecalis increased significantly, while the number of viable colonies of Campylobacter, Bifidobacterium, and Lactobacillus decreased significantly, with statistical significance (P < 0.05).

Figure 3.

Comparison of flora distribution between intestinal cancer patients after surgery and healthy controls.

Growth curves of intestinal flora in patients with colorectal cancer with and without heparin

Figure 4 shows the growth of biofilm formation under different heparin concentrations. As the concentration of heparin added to the medium increased, the amount of biofilm formed by bacteria also increased, showing a significant positive correlation trend. It was verified that Heparin can promote the formation of biofilm of bacteria with a dose effect.

Figure 4.

Growth of biofilm formation under different heparin concentrations.

Figure 5 shows the biofilm images in the medium of three groups with different heparin concentrations. With the increase of heparin concentration, the biofilm density of bacteria in the medium increased significantly.

Figure 5.

Biofilm images in three groups of heparin medium with different concentration gradient. (a: 5 mg/mL heparin medium; b: 10 mg/mL heparin medium; c: 15 mg/mL medium.)

The growth curve of intestinal flora in patients with colorectal cancer

Figure 6 shows the growth curve of intestinal flora in patients with colorectal cancer. In the medium with and without heparin, there was no significant difference in the growth of bacterial community in each period (P > 0.05), which meant that whether adding heparin in the medium did not affect the growth of bacterial strains.

Figure 6.

Growth curves of intestinal flora in patients with intestinal cancer.

Serum D-lactic acid levels of cancer patients before and after operation

Figure 7 shows the comparison of serum D-lactic acid level between the control group and the experimental group before and after operation. The serum D-lactic acid concentration in colorectal cancer group was (1.41 ± 0.39) μg/mL before operation, (6.38 ± 1.42) μg/mL after operation, and (0.91 ± 0.52 μg/mL compared with healthy control group. Compared with the control group, serum D-lactic acid level in the experimental group was significantly different before and after operation (P < 0.05).

Figure 7.

Serum D-lactic acid levels of patients with colorectal cancer of control group and experimental group before and after operation.

The levels of endotoxin in the control group and the experimental groups before and after operation

Figure 8 shows the comparison of endotoxin levels between the control group and the experimental group before and after operation. The level of endotoxin was (0.62 ± 0.09) EU/mL in the colorectal cancer group before surgery, (0.80 ± 0.15) EU/ mL in the colorectal cancer group after surgery, and (0.05 ± 0.02) EU/mL in the control group. After comparison, the endotoxin level of the experimental group was significantly higher than that of the control group before and after surgery, with statistical significance (P < 0.05).

Figure 8.

Comparison of endotoxin levels between the control group and the experimental group before and after operation.

Discussion

Epidemiological investigation showed that the incidence and mortality of colon cancer in China remain high every year, and the urban incidence and mortality are also increasing rapidly. The pathogenesis of colon cancer is very complex, and the disturbed intestinal environment is one of the key factors leading to colon cancer. It is extremely important to maintain a relatively stable state of the type and quantity of normal human intestinal flora. Once the balance is broken, opportunistic infections or nutrient malabsorption will be caused [16,17]. In addition, studies found that the balanced microbiome of intestinal flora can protect immune function, and transplanting human intestinal microbes can achieve the purpose of treating inflammatory bowel disease, metabolic syndrome, and other diseases [18,19].

The results showed that, compared with the healthy control group, the number of live bacteria colonies of Escherichia coli and Enterococcus faecalis increased significantly in the preoperative and postoperative flora distribution of patients in the colorectal cancer group. The number of live bacteria colonies of Campylobacter, Bifidobacterium, and Lactobacillus decreased significantly, with statistical significance (P < 0.05). These results indicated that the changes of intestinal flora were closely related to intestinal lesions. This was consistent with the research results of de Andrade Calaça et al. (2017) [20], which all believed that patients with colorectal cancer will have a very obvious imbalance of intestinal flora. In addition, the comparison of serum D-lactic acid level and endotoxin level between the control group and the experimental group before and after operation showed that the serum D-lactic acid level of the experimental group (1.41 ± 0.39 μg/mL, 6.38 ± 1.42 μg/mL) was significantly higher than that of the control group (0.91 ± 0.52 μg/mL) before and after operation, with statistical significance (P < 0.05). In addition, the endotoxin levels of colorectal cancer patients in the experimental group (0.62 ± 0.09 EU/mL, 0.80 ± 0.15 EU/mL) were significantly higher than those in the control group (0.05 ± 0.02 EU/mL), and the difference was statistically significant (P < 0.05). Therefore, the levels of D-lactic acid and endotoxin in serum of patients with colorectal cancer were significantly higher than those of healthy people. Current studies suggested that D-lactic acid and endotoxin, as substances produced by intestinal flora, can not migrate into the bloodstream through non-cancer or intact intestinal mucosa. However, when intestinal membrane barrier function is impaired, serum D-lactic acid and endotoxin levels will increase [21]. This indicates that bowel cancer may have abnormal signal transduction mechanism in response to intestinal mucosa, and the pro-inflammatory signal cannot be transmitted correctly, resulting in severe damage to intestinal mucosa epithelium, which leads to cancer. However, impaired intestinal membrane barrier function can cause changes in serum D-lactic acid and endotoxin levels [22].

The experimental results of intestinal flora biofilm in patients with colorectal cancer under different heparin levels showed that with the increase of heparin concentration in the medium, the amount of biofilm formed by bacteria also increased, presenting a significant positive correlation trend. Under the microscope, a significant increase in the density of bacterial biofilm was seen, which indicated that heparin can promote the formation of bacterial biofilm, and its promoting effect showed a certain dose effect. In addition, in the medium with and without heparin, there was no significant difference in the growth of bacterial community in each period (P > 0.05), which indicated that adding heparin did not affect the growth of intestinal bacterial strains in patients with colorectal cancer but increased the growth of biofilm. This study demonstrated that heparin had a positive effect on bacterial colony formation of biofilm, which may provide a new idea for using biofilm resistance to protect intestinal mucosa. Heparin is synthesized in the endoplasmic reticulum of animal somatic cells and the Golgi apparatus of mast cells. Studies reported that heparin can stimulate the formation of bacterial biofilms in vitro, such as Staphylococcus aureus [23]. The formation of biofilm can form a protective layer in the intestinal tract of patients, which plays a positive role in the treatment of colorectal cancer. In addition, this study found that heparin can promote the formation of bacterial biofilm, and the promoting effect of heparin on the formation of bacterial biofilm did not depend on the promotion of bacterial strain growth.

Conclusion

This study aimed to explore the influence of abnormal intestinal flora on the risk of colorectal cancer by comparing the intestinal flora differences between patients with colorectal cancer and healthy subjects. The influence of heparin on the formation of microbial biofilm was investigated by studying the growth of microbial biofilm under different heparin concentration gradients. The results showed that there were significant differences in intestinal flora between colon cancer patients and healthy patients (P < 0.05). The serum D-lactic acid level and endotoxin level of patients in the experimental group were significantly higher than those in the control group before and after operation, with statistical significance (P < 0.05). With the increase of heparin concentration in the medium, the amount of biofilm formed by bacteria also increased, showing a significant positive correlation, but it had no effect on the growth of intestinal bacterial colony in patients with colorectal cancer with or without heparin (P > 0.05). However, the limitation of this study is that the specific mechanism of heparin affecting the growth of bacterial biofilm was not discussed. Subsequently, the relationship between heparin structure and promoting bacterial biofilm formation will be explored based on the structural similarity between heparin and capsular polysaccharide. All in all, the results of this study provide a good theoretical basis for the study of the relationship between intestinal cancer pathogenic bacteria and biofilms.