Mechanism and Process Regulation for Colorectal Tumors

Inclusion Criteria:

* Inclusion Criteria（Healthy control group）： 1) Aged more than 18 years; 2) Planned to undergo colonoscopy , without past medical history of neoplasm or ulcer or bleeding under colonoscopy regardless of the history of colonoscopy; 3) Willing to participate in this trial and signed the informed consent.

  * Inclusion Criteria（Sporadic colorectal adenoma group）：

    1. More than 18 years aged;
    2. Diagnosed as colorectal adenoma, epithelial adenomatoid hyperplasia, serrated lesions, or with mild to moderate dysplasia (low-grade intraepithelial neoplasia) by colonoscopy and pathology;
    3. Signed the informed consent, willing to participate in this trial.
  * Inclusion Criteria（Sporadic early colorectal cancer group）：

    1. Aged more than 18 years;
    2. Underwent endoscopic EMR/ESD or Surgical resection because of colorectal neoplasms and the lesion was confined to the mucosa or submucosa of the large intestine and was pathologically indicated to be adenocarcinoma;
    3. Willing to participate in this trial and signed the informed consent.
  * Inclusion Criteria（Familial colorectal neoplasm group）：

    1. Aged more than 18 years;
    2. Underwent ESD/EMR resection or surgical resection and the pathology result considered as early colorectal cancer and adenoma, and the family history, pathology and genetic tests met the diagnostic criteria of FAP and HNPCC/LS;
    3. Signed the informed consent, willing to participate in this trial. ·-Inclusion Criteria (Cohort study)

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    1. Aged 18-80 years;
    2. Diagnosed as polypoid neoplasm or lateral developmental neoplasm (LST) by endoscopy without a family history of CRC and the pathologic manifestations were conventional adenoma or serrated lesions; the patients without a family history of CRC underwent ESD or EMR resection and the pathology result considered as early colorectal cancer; diagnosed as sporadic colorectal early carcinoma and adenoma with a family history of colorectal cancer (FAP, Lynch syndrome);
    3. Signed the informed consent, willing to participate in this study and agreed with colonoscopy with pathology examination once a year and followed up for 5 years.

Exclusion Criteria:

* -Exclusion Criteria（Healthy control group）：

  1. With a medical history of digestive tract rerouting and partial resection;
  2. Patients with high risk of hereditary colorectal adenocarcinoma, i.e. family members of the following diseases: family history of gastrointestinal neoplasms, familial adenomatous polyposis (FAP), hereditary non-polyposis colorectal adenocarcinoma (HNPCC/LS), and P-J syndrome;
  3. With A history of chronic metabolic and inflammatory diseases such as hypertension, diabetes, chronic viral hepatitis, and inflammatory bowel disease and the chronic disease were difficult to control;
  4. With other malignancies known to have advanced or require treatment in the past 5 years, except basal cell and squamous cell carcinoma of the skin that have been radically cured;
  5. With a history of active gastrointestinal bleeding within the last 6 months;
  6. With a history of using broad-spectrum antibiotics and probiotics by oral or intravenous within the past 1 month;
  7. Received routine immunosuppressive drugs for the past 6 months;
  8. Unable or unwilling to cooperate with follow-up and related examinations;
  9. Patients who can not eat normally or need to rely on medicine or enema and other defecation;
  10. With mental illness or any other serious cardiovascular disease;
  11. With pregnant or lactating or planning to become pregnant within one year;
  12. Currently participating in, or receiving, an interventional clinical study that affects patients' treatment decisions.
* Exclusion Criteria（Sporadic colorectal adenoma group）：

  1. With a medical history of digestive tract rerouting and partial resection;
  2. Patients with high risk of hereditary colorectal adenocarcinoma, i.e. family members of the following diseases: family history of gastrointestinal neoplasms, familial adenomatous polyposis (FAP), hereditary non-polyposis colorectal adenocarcinoma (HNPCC/LS), and P-J syndrome;
  3. With A history of chronic metabolic and inflammatory diseases such as hypertension, diabetes, chronic viral hepatitis, and inflammatory bowel disease and the chronic disease were difficult to control;
  4. With other malignancies known to have advanced or require treatment in the past 5 years, except basal cell and squamous cell carcinoma of the skin that have been radically cured;
  5. With a history of active gastrointestinal bleeding within the last 6 months;
  6. With a history of using broad-spectrum antibiotics and probiotics by oral or intravenous within the past 1 month;
  7. Received routine immunosuppressive drugs for the past 6 months;
  8. Unable or unwilling to cooperate with follow-up and related examinations;
  9. Patients who can not eat normally or need to rely on medicine or enema and other defecation;
  10. With mental illness or any other serious cardiovascular disease;
  11. With pregnant or lactating or planning to become pregnant within one year;
  12. Currently participating in, or receiving, an interventional clinical study that affects patients' treatment decisions.
* Exclusion Criteria（Sporadic early colorectal cancer group）：

  1. With a medical history of digestive tract rerouting and partial resection;
  2. Patients with high risk of hereditary colorectal adenocarcinoma, i.e. family members of the following diseases: family history of gastrointestinal neoplasms, familial adenomatous polyposis (FAP), hereditary non-polyposis colorectal adenocarcinoma (HNPCC/LS), and P-J syndrome;
  3. With A history of chronic metabolic and inflammatory diseases such as hypertension, diabetes, chronic viral hepatitis, and inflammatory bowel disease and the chronic disease were difficult to control;
  4. With other malignancies known to have advanced or require treatment in the past 5 years, except basal cell and squamous cell carcinoma of the skin that have been radically cured;
  5. With a history of active gastrointestinal bleeding within the last 6 months;
  6. With a history of using broad-spectrum antibiotics and probiotics by oral or intravenous within the past 1 month;
  7. Received routine immunosuppressive drugs for the past 6 months;
  8. Unable or unwilling to cooperate with follow-up and related examinations;
  9. Patients who can not eat normally or need to rely on medicine or enema and other defecation;
  10. With mental illness or any other serious cardiovascular disease;
  11. With pregnant or lactating or planning to become pregnant within one year;
  12. Currently participating in, or receiving, an interventional clinical study that affects patients' treatment decisions.
* Exclusion Criteria（Familial colorectal neoplasm group）：

  1. With a medical history of digestive tract rerouting and partial resection;
  2. With A history of chronic metabolic and inflammatory diseases such as hypertension, diabetes, chronic viral hepatitis, and inflammatory bowel disease and the chronic disease were difficult to control;
  3. With a history of active gastrointestinal bleeding within the last 6 months;
  4. With a history of using broad-spectrum antibiotics and probiotics by oral or intravenous within the past 1 month;
  5. Received routine immunosuppressive drugs for the past 6 months;
  6. Unable or unwilling to cooperate with follow-up and related examinations;
  7. Patients who can not eat normally or need to rely on medicine or enema and other defecation;
  8. With mental illness or any other serious cardiovascular disease;
  9. With pregnant or lactating or planning to become pregnant within one year;
  10. Currently participating in, or receiving, an interventional clinical study that affects patients' treatment decisions.

      * Exclusion Criteria（Cohort study）

Except baseline exclusion criteria, and the following conditions should be excluded:

1. Diagnosed as advanced colorectal cancer (with or without surgery, radiation, chemotherapy, targeted therapy, immunotherapy);
2. Refuse to sign the informed consent.