Background:
Colorectal cancer (CRC) is a high-indence malignance of the digestive
system with a high mortality rate in the world.
Aim:
The results are desired to provide an important theoretical basis for discovering new therapeutic
targets for CRC.
Objective:
The expression of human endogenous retrovirus-H-long terminal repeat association protein
2 (HHLA2) in human CRC was detected to explore its correlationship with clinicopathological
features and prognosis of patients and its potential in treating CRC.
Methods:
Western blot was employed to detect HHLA2 expression in fresh tissues obtained from
6 CRC patients' excisions, including cancer, paracancer, and normal issues. Immunohistochemical
staining was employed to determine HHLA2 expression in paraffin-embedded specimens of 139
patients with colorectal cancer, and its relationship with the clinicopathological profiles and survival
was analyzed. Small interfering RNA (siRNA) targeting HHLA2 was used to transfect CRC
cells to silent HHLA2. MTT, plate colony formation, cell scratch, and Transwell assay were conducted
to observe the proliferation, migration, and invasion of CRC cells.
result:
HHLA2 protein was expressed in human colorectal cancer tissues, paracancer tissues and normal tissues, and its expression significantly upregulated in cancer tissues (P<0.01). HHLA2 expression level in colorectal cancer tissues showed a close correlationship with the invasion depth of tumor (P=0.000), metastasis of regional lymph nodes (P=0.018), clinical stage (P=0.010) and patient survival (P=0.011). No significant correlation was found with gender (P=0.873), age (P=0.864), location of tumor (P=0.768), degree of tumor differentiation (P=0.569) and distant metastasis (P=0.494). Survival analysis showed that the survival time of colorectal cancer patients with high and low HHLA2 expression group was 43.231 months and 55.649 months, respectively, with statistical difference between the two groups (P=0.001). HHLA2 silencing significantly inhibited the proliferation, migration and invasion of CRC cells.
Results:
HHLA2 protein was expressed in human colorectal cancer tissues, paracancer tissues and
normal tissues, which was significantly upregulated in cancer tissues (P<0.01). HHLA2 expression
level in CRC tissues showed a close correlationship with the invasion depth of the tumor
(P=0.000), metastasis of regional lymph nodes (P=0.018), clinical stage (P=0.010), and patient survival
(P=0.011). Correlation with gender (P=0.873), age (P=0.864), location of the tumor
(P=0.768), degree of tumor differentiation (P=0.569) and distant metastasis (P=0.494) exhibited
no significance. The survival time of CRC patients with high and low HHLA2 expression groups
was 43.231 months and 55.649 months, respectively, with a statistical difference between the two
groups (P=0.001). Silencing HHLA2 inhibited proliferation, migration and invasion of CRC cells
significantly.
Conclusion:
HHLA2 is overexpressed in CRC tissues which is associated with poor prognosis of
patients. HHLA2 might be recognized as a new candidate for adjuvant diagnosis and prognosis of
CRC, as well as a promised new target for immunotherapy of CRC.
other:
no