Hereditary colorectal cancer in china.

The purpose of this article is to review basic research as well as clinical studies on Chinese hereditary colorectal cancer. Hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) accounts for 2.2% of all colorectal cancer, and Chinese criteria for suspected HNPCC have been developed. Germline mutations as well as large genomic rearrangements of mismatch repair (MMR) genes are responsible for this syndrome. Gastric cancer is the second most common cancer in Chinese HNPCC patients. Contrary to sporadic colorectal cancer in the Chinese population, HNPCC does not typically present with rectal cancer. Incidence of familial adenomatous polyposis (FAP) in China is approximately 1.5/100,000. Polyps in Chinese FAP patients can emerge as early as 16 months old, but malignant transformation usually occurs in the third and fourth decade. Total resection of the colon and rectum is necessary in FAP patients. For unresectable duodenal polyps, chemopreventive agents may be used.

Introduction

According to the IACR (International Association of Cancer Registries) [1], in the year 2002, 150,956 new cases of colorectal cancer (CRC) were expected to occur in China, while the age-standardised incidence of colorectal cancer would be 13.6/100,000 in men and 9.3/100,000 in women. These predictions were derived from cancer statistics of six separate areas in China from 1993 to 1997. However, in 1999 colorectal cancer incidence in Shanghai, the biggest city in China included in the IARC's estimates, had already reached 16.2/100,000 in men and 14.5/100,000 in women [2], more than a one-fold increase compared with the 1972-1974 period [3]. Shanghai has witnessed the highest and fastest growing colorectal cancer incidence in China. It is a fact that the incidence of colorectal cancer in China is increasing rapidly.

Genetic alterations as well as environmental influences are thought to underlie the development of all colorectal malignancies. In general, environmental changes play a critical role in the rapid growth of colorectal cancer incidence, while the contribution of genetic alterations that cause hereditary colorectal cancer is probably relatively stable. Although there are no statistics available on the incidence of hereditary colorectal cancer in China as a whole, we expect that the incidence of hereditary colorectal cancer in China is growing due to the changing environment as well as to more diagnosed cases because of more clearly specified diagnostic criteria. According to Lynch et al. [4], approximately 20% of all patients with colorectal cancer carry a familial risk, with 5-10% inherited as a Mendelian trait. Hereditary colorectal cancer can be broadly classified into two categories based on the presence or absence of multiple colorectal polyps: polyposis syndromes and nonpolyposis syndromes. The former can be further divided on the basis of histologic criteria into adenomatous-like FAP and hamartomatous syndromes like juvenile polyposis and Peutz-Jeghers syndrome. This article will review clinical and basic research on both types of hereditary colorectal cancer syndromes in China, focusing on the differences with Western countries and particular characteristics of Chinese hereditary colorectal cancer. Relevant new issues on hereditary colorectal cancer outside China will also be discussed.

Hereditary nonpolyposis colorectal cancer (HNPCC)

HNPCC, which some prefer to refer to as Lynch syndrome, is an autosomal dominant inherited cancer syndrome caused by germline mutations of mismatch repair (MMR) genes. This disorder is characterised by early onset of colorectal cancer and other malignancies including gastric, endometrial, ovarian, ureter, renal pelvis, hepatobiliary tract and small bowel cancer. When the name Lynch syndrome was first coined by Borland in 1984 [5], a Lynch family with five cases was reported in the same year in a Chinese medical journal [6], but it was not until 1998 that a series of Chinese HNPCC families began to be studied [7]. Several research groups in China have been devoted to collecting and studying Chinese Lynch families. With their effort, clinical and molecular research on HNPCCs in China has been greatly accelerated.

Clinical diagnosis

The diagnostic criteria for HNPCC continue to evolve as the understanding and characteristics of this heterogeneous disorder improve. The Amsterdam criteria, which were established in 1990 and revised in 1999, have been the classical diagnostic criteria of HNPCC. Based on the Amsterdam criteria, HNPCC in China accounts for 2.2% of all colorectal cancer [8]. However, the Amsterdam criteria are too strict for diagnostic purposes or for exclusion of patients from further work-up. More importantly, they do not account for patients from small families, which is a common phenomenon in China. With these deficiencies in mind, several sets of modified clinical criteria such as the Bethesda criteria [9], revised Bethesda criteria [10], Japanese criteria [11] and Korean suspected criteria [12] have been proposed. The National Hereditary Colorectal Cancer Network of China proposed Chinese HNPCC criteria in 2003 [13]. Based on the Korean suspected criteria, Chinese HNPCC criteria have been modified as follows: at least two pathologically verified colorectal cancers in a family; at least two of them are first-degree relatives including parents or siblings; in addition, at least one of these conditions has to be satisfied: (1) at least one case develops multiple colorectal cancer, including adenomas, (2) at least one colorectal cancer is diagnosed before age 50, (3) at least one case with extracolonic malignancies including gastric, endometrial, small bowel, ureter and renal pelvis, ovarian, and hepatobiliary malignancies. The differences between Chinese criteria and other criteria are listed in Table 1.

Table 1

Comparison of clinical diagnostic criteria for HNPCC

Criteria Items colorectal cancer patients	Amsterdam criteria (including I and II) ≥3 (including extracolonic tumours)	Japanese criteria A ≥3	Chinese criteria ≥2	Japanese criteria B ≥2	Bethesda guidelines (2004) ≥1
first-degree relatives	at least 2 pairs	at least 2 pairs	at least 1 pair	at least 1 pair	no request
generations affected	at least 2 successive generations	no request	no request	no request	no request
exclude FAP	yes	no request	no request	no request	no request
with any of these:	at least 1 should be diagnosed before age 50	no request	at least 1 should be diagnosed before age 50	at least 1 should be diagnosed before age 50	CRC diagnosed before age 50
			multiple colorectal tumors (including adenomas)	multiple colorectal cancers	Multiple colorectal tumors
			extracolorectal cancer	extracolorectal cancer	HNPCC-associated tumours
				right colon involvement	MSI-H pathologic associated features in a colorectal cancer diagnosed before age 60
					- one with colorectal cancer- one or more first- or second-degree relatives with HNPCC-related tumour- one of the cancers being diagnosed before age 50
					- one with colorectal cancer- two or more first- or second-degree relatives with HNPCC-related tumour

Note: MSI-H pathologic associated features including the presence of tumor infiltrating lymphocytes, Crohn's-like lymphocytic reaction, mucinous/signet-ring differentiation, or medullary growth pattern

Genetics

Since the discovery of the major human gene with DNA misrepair function in 1993-1995, mutations in MSH2, MLH1, MSH6 and PMS2 have been convincingly associated with HNPCC. According to the database maintained by the international collaborative group on HNPCC (International Society for Gastrointestinal Hereditary Tumor, InSiGHT), approximately 450 different HNPCC-associated mismatch repair gene mutations are known that primarily involve MLH1 (~50%), MSH2 (~39%), and MSH6 (~7%) [14]. Most of these mutations are frameshift and nonsense mutations which are obviously pathogenic, but the roles missense mutations play are diversified. Some may be harmless single nucleotide polymorphisms, whereas others may contribute to cancer risks. Studying segregation of these mutations in affected and unaffected relatives, and functional assays, are among the methods to investigate the functional nature of these missense mutations. In addition to these point mutations, large genomic rearrangements of MMR genes have recently been reported to play an important role in the development of HNPCC. A systematic search of 439 HNPCC families for genomic rearrangements in MSH2, MLH1, MSH6 and PMS2 has identified 48 genomic rearrangements in 68 unrelated kindreds. Twenty-nine out of 48 were found in MSH2, 13 in MLH1, 2 in MSH6, and 4 in PMS2 [15].

For the purpose of presenting the genetic alterations in Chinese HNPCC families, eight doctorate studies [16-23] which aimed at germline mutation detection in Chinese HNPCC have been summarised. A total of 35 clinically diagnosed unrelated HNPCC families, most of them meeting Amsterdam criteria, have been found to carry 43 germline mutations (60% MLH1 mutations and 40% MSH2 mutations (Table 2). All of the genomic sites of mutations were verified by DNA sequencing. Among these mutations, 10/43 (23%) result in a shift of transcribe reading frame. Eight out of forty-three (19%) are nonsense mutations which lead to truncating proteins. These are obviously pathological mutations. However, missense and splice site mutations, which account for 14/43 (33%) and 7/43 (16%), respectively, are putative mutations needing further pathological verifications. Four of the observed mutations were small nucleotide deletions, which may help in discovering the critical amino acid related functions of MMR proteins. In addition to small mutations, large genomic rearrangements of Chinese HNPCC are also investigated. Huang et al. first reported a genomic deletion ranging from exon 1 to exon 7 of MSH2 gene in a Chinese HNPCC family meeting Amsterdam criteria [24]. A recent study [25] shows that large genomic rearrangements, mostly deletions rather than duplications, were responsible for 7 out of 45 hereditary colorectal patients. These large fragment aberrations, uncovered in both MSH2 and MLH1, indicate that large genomic rearrangements play a role in the pathogenesis of Chinese hereditary CRC patients. So far, the genetic alterations in Chinese HNPCC appear similar to those in Western countries; however, there are no data yet on the prevalence of Chinese MSH6 and PMS2 gene mutations.

Table 2

Germline MLH1 and MSH2 mutations observed in Chinese HNPCC families

Family	Criteria	mutation in:		mutation type	reference
		MLH1	MSH2
C4	Amsterdam	E18 c.2081 int T	E15 c.2469 int C	frameshift	[16]
			c.2471 int G	frameshift
			c. 2578 int T	frameshift
C11	Amsterdam	E13 c.2091 T>A		nonsense	[16]
C13	Amsterdam	E11 c.1760int T		frameshift	[16]
		c.1688 A>C		missense
H2	Amsterdam	E13 c.2038 C>T		nonsense	[17]
H4	Amsterdam	E2 c.199 A>G		missense	[18]
H9	Amsterdam	E11 c.305 del 24bp		small deletion	[17]
H11	Amsterdam		E1 c.14 A>C	missense	[17]
H27	Amsterdam		E3 c.617 int A	frameshift	[17]
N8	Amsterdam	E8 c.655 A>G		missense	[19]
N11	Amsterdam	E3 c.265 G>T		nonsense	[19]
N14	Amsterdam	E6 c.545+3 A>G		splice point	[19]
N23	Amsterdam	E3 c.610 G>T		nonsense	[19]
N25	Amsterdam	E8 c.677 G>A		missense	[19]
HW7	Amsterdam	E14 c.2228 C>A		nonsense	[20]
HW5	Amsterdam	E14 c.1588-1590 del		small deletion	[20]
C1	Japan	E11 c.934 int A		frameshift	[21]
C6	Japan	E1 c.21 G>C		missense	[22]
C8	Japan	E12 c.1198 C>G		missense	[21]
		c.1261 C>G		missense
		c.1364 int C		frameshift
		c.1372 int C		frameshift
N18	Japan	E9 c.790+1 G>A		splice point	[19]
N26	Japan		E14 c.2211-2 A>C	splice point	[19]
HW6	Japan	E15 c.1731+1 A>G		missense	[20]
H12	China	E15 c.2516 G>A		missense	[18]
H20	China	E19 c.2250 G>C		nonsense	[18]
H5	*		E3 c.425 G>C	nonsense	[23]
H6	*	E15 c.1731 G>A		splice point	[23]
H17	*	E15 c.1731 G>A		splice point	[23]
H45	*	E16 c.1846 del AAG		small deletion	[23]
H47	*	E12 c.1151 T>A		missense	[23]
H52	*	E2 c.194 G>A		missense	[23]
H56	*		E16 c.2792 A>C	missense	[23]
H62	*	E14 c.1588 del TTC		small deletion	[23]
H64	*	E15 c.1731+1 G>A		splice point	[23]
H65	*	E14 c.2228 C>A		nonsense	[23]
H67	*	E14 c.1559-2 G>A		splice point	[23]
H68	*	E2 c.137 G>T		missense	[23]
		E11 c.914 int 24		frameshift	[23]

E = exon, c = codon

* = clinical diagnostic criteria for each of these families are unknown, but it is clear that one of them meets the Bethesda criteria and three of them meet the Japanese criteria

In the Chinese studies, colorectal cancer patients were selected for germline mutation detection, more frequently using criteria for suspected HNPCC rather than the Bethesda criteria. Table 3 shows different detection rates of germline mutations in typical and suspected HNPCC families. The highest rate was observed in kindreds meeting the Amsterdam criteria, which is about 44%, similar to that in reports from Western countries, which often quote a rate between 40% and 60%. Compared with the Bethesda criteria, we prefer to use the suspected HNPCC criteria in the clinical setting of screening for HNPCC. Especially in small Chinese families we would suggest using the suspected HNPCC criteria rather than the Amsterdam criteria.

Table 3

Rates of detected germline MLH1 and MSH2 mutations in Chinese typical and suspected HNPCC patients

Clinical Criteria	positive/screened	percentage	reference
Amsterdam	23/52	44%	[18-20,22,23]
Japan	8/24	33%	[19,20,22]
Korea/China	5/23	22%	[18]*
Bethesda	1/19	5%	[22]

* partly based on unpublished data

Clinical manifestations

The most striking feature of HNPCC is the predisposition for early onset and/or multiple colorectal malignancies. The mean age of onset of colorectal cancer is 44 years, approximately 20 years earlier than that for sporadic colorectal cancer. In Lynch families, colorectal cancer tends to be multiple, either synchronously (18%) or metachronously (24%) [26]. Other features of HNPCC involve proximal location of CRC, mucinous or poorly differentiated histology, and better prognosis. Previous studies [16,27-48] have shown features of colorectal cancer in Chinese HNPCC patients (Table 4). With a few exceptions, clinical manifestations of Chinese HNPCC colorectal cancer are largely the same as those described above. However, the involvement of rectal cancer in HNPCC is the most interesting exception. Contrary to sporadic CRC in the Western world, more than half of colorectal cancer in China is rectal cancer rather than colon cancer. But this distribution does not exist in colorectal cancer in HNPCC families. Although they account for less than half of all cases of colorectal cancer, rectal cancer in Lynch families is considerably reduced compared with sporadic CRCs. This may indicate differences in oncogenetic pathways between HNPCC and sporadic CRCs.

Table 4

Features of colorectal cancer In Chinese HNPCC and sporadic CRC patients

	Amsterdam criteria cases (%)	Japanese criteria cases (%)	Chinese/Korean criteria cases (%)	Sporadic CRC cases (%)
1. Gender
male	166 (55)	53 (48)	14 (33)	437 (47)
female	136 (45)	57 (52)	28 (67)	50 (53)
2. Location
right colon	85 (40)	33 (26)	144 (10)
other colon	155 (73)	65 (52)	26 (62)	540 (39)
rectum	57 (27)	60 (48)	16 (38)	853 (61)
3. Duke's stage
A&B	67 (63)	42 (46)	34 (81)	387 (49)
C&D	40 (37)	49 (54)	8 (19)	400 (51)
4. Differentiation
low grade	17 (40)	24 (39)	5 (13)	108 (14)
high grade	25 (50)	38 (61)	34 (87)	664 (86)
5. Multiple malignancy
total	25 (9)	19 (15)	6 (14)	25 (3)
synchronous	5 (2)	11 (9)
metachronous	20 (7)	8 (6)
not multiple	260 (91)	110 (85)	36 (86)	867 (97)
6. Adenomas
with adenomas	13 (18)	6 (21)	98 (18)
without adenomas	58 (82)	23 (79)	450 (82)

Lynch syndrome is associated with a wide spectrum of cancers. The pattern of cancers has changed over time. Previous studies [49] indicate that there are several ways to verify whether or not a particular tumour may be associated with HNPCC. A demonstrated increase in risk of developing a particular tumour type in HNPCC families (or better, proven mutation carriers) is the classical approach taken. Based on these principles, the recent Bethesda conference advised that colorectal, endometrial, gastric, ovarian, small bowel, hepatobiliary, ureter and renal pelvis cancer should be included in the HNPCC-associated tumour spectrum [10]. However, the tumour spectrum of HNPCC families from Western countries is quite different to that from the Far East. This reflects the variation in incidence of cancers in the respective populations. For example, gastric cancer instead of endometrial cancer is the second most common cancer in Chinese Lynch syndrome families. Among 30 Amsterdam families, 10 out of 27 extracolonic malignancies involved gastric cancer, much more than the 4 cases of endometrial cancer [50]. Because no difference in clinical manifestation between HNPCC-associated gastric cancer and familial gastric cancer has been found [51], further studies of germline mutations of HNPCC-associated gastric cancer are needed.

Management and surveillance

Identification of families with HNPCC syndrome based on exact clinical information is inefficient according to the genetic definition of HNPCC. Even when the original Amsterdam criteria are met in a family, the likelihood of detecting a germline mismatch repair gene mutation is only 40-60% [52]. However, one of the main benefits of genetic analysis is the identification of mutation negative family members in a positive pedigree, since it frees the individual from anxiety and unnecessarily frequent surveillance. An algorithm (Fig. 1) for the genetic screening of individuals suspected for HNPCC has been established by the National Hereditary Colorectal Cancer Network of China [13]. Microsatellite instability (MSI) and immunohistochemistry (IHC) testing for MMR genes in tumour tissue is used as a complementary screening method. Individuals with negative results are excluded from further genetic testing.

Figure 1

Genetic Screening Strategy for HNPCC in China.

Once suspected HNPCC has been diagnosed, 7-10 ml of peripheral blood of the patient are collected. 3 ml of this sample are used for white blood cell immortalization, and the rest is stored in a -20°C refrigerator for further study. Subsequently, clinical screening takes place, including detailed endoscopic examination of the whole gastrointestinal tract, followed by ultrasound screening of the pelvis and hepatobiliary organs. A regular surgical operation is performed if a tumour is detected. Although multiple malignancies in the colon and rectum are not infrequent in HNPCC, prophylactic colectomy is still not recommended. Recent studies [53] show that HNPCC colorectal cancers, which are usually microsatellite intsable, are insensitive to 5-FU-based chemotherapic regimens; however, adjuvant chemotherapy after colonectomy is still routinely prescribed.

For patients with cancer or affect individuals with a definitive inherited mutation, interval surveillance is recommended for colorectal, gastric and endometrial cancer. Data have shown [54] that lifetime risks for colorectal, gastric and endometrial cancer in Chinese HNPCC are 93.3%, 28.1% and 23.3% respectively. Although these cancer risks might be overestimated, surveillance for these malignancies is necessary. Considering the early onset of HNPCC malignancies and the tendency for proximal and metachronous colon lesions, full colonoscopy is recommended every one to two years beginning between the ages of 20 and 25. Removal of polyps can also be undertaken during endoscopic examination, which likely reduces the risk of colorectal cancer and may prolong survival. Other reasonable approaches involve transvaginal ultrasound or endometrial aspiration with cytology to screen for endometrial cancer and gastroendoscopy for gastric cancer, based on available evidence and expert opinions.

Familial adenomatous polyposis (FAP)

FAP is an autosomal dominantly inherited disease with almost 100% penetrance characterised by the presence of hundreds to thousands of small adenomatous polyps, which if left untreated would almost certainly develop into colorectal cancer. Mutations in the adenomatous polyposis coli (APC) gene are responsible for the syndrome. In addition, several variants of the syndrome exist, namely Gardner syndrome, Turcot syndrome and attenuated adenomatous polyposis (AAPC or AFAP). Compared with HNPCC, fewer research papers have been published on FAP in China.

Incidence

In China, of all colorectal cancer, only 0.94% is due to FAP. According to a survey executed twenty years age in a county in the south-east of China, the incidence of FAP in 18,950 individuals above age 30 was estimated to be approximately 1.5/100,000 [55]. However, this was an outcome after screening by 15cm rectum endoscopy; therefore the real incidence in this county would probably be a little higher.

Clinical features

The hallmark of FAP is the growth of profuse adenomatous colorectal polyps at a young age. Diarrhoea, gastrointestinal bleeding and abdominal pain caused by polyps lead to the diagnosis. The polyps in FAP have a slight predisposition for the distal colon. However, the most important feature in Chinese FAP is the incidence of rectum polyps. Among 42 FAP patients in their first visit to the hospital, 30 were found to have polyps in rectums simply by anal and rectum check by finger, which finally led to the diagnosis of FAP [56]. Polyps can emerge in FAP patients as young as 16 months in China [57]. The number and size of these polyps increases with time, ultimately reaching the number of hundreds to thousands. If left untreated, nearly all patients with this disorder will ultimately develop colorectal cancer due to the vast number of polyps. Liu Jian et al. [55] collected 50 FAP families in the 1979-1993 period. FAP was diagnosed at the average age of 31 years. Sixty-four percent of the patients had developed colorectal cancer. After endoscopic screening of 57 first-degree relatives, another 18 FAP patients, with an average age of 19 years were uncovered. Only 5.65% of these new-found FAP cases had developed colorectal cancer, significantly lower than that of the index cases. This shows that cancer risk for Chinese FAP increases rapidly in the course of time, especially during the third and fourth decades of life. As in Western populations, age is the determinant of cancer risk in Chinese FAP patients as well.

APC gene mutation

Mutations in the APC gene are responsible for this syndrome. In most cases, one allele with the mutated gene is inherited from an affected parent. An acquired (somatic) mutation in the other APC allele results in the development of adenomas. However, a lack of family history can be observed in one third of cases, which is explained by de novo germline mutations. It has been reported that an APC gene mutation can be detected in 80-90% of FAP patients [58]. Gan Yuebo et al. [59] first reported an APC germline mutation in Chinese FAP patients in 1994. One out of 7 APC families was found to have an AAAGA nucleotide deletion in codon 1309-1311. Recently, studies on the large exon 15 of APC were reported. Five out of 22 FAP pedigrees were found to have germline mutations in this exon, all them being frameshift mutations [60]. Another study reported 6 out of 18 FAP patients having germline mutations on 4 fragments in exon 14 and 15 [61]. Recently, germline mutations in the MYH gene have been identified as another cause of adenomatous polyposis. The role of MYH in Chinese (A) FAP has not been studied yet.

Management and prevention

After the clinical diagnosis of FAP, prophylactic colostomy is recommended. However, the optimal timing for this procedure is difficult to specify. The balance between disease progression and the adolescent's physical and psychosocial maturity should be considered. Presently, the surgical methods in China involve total resection of the colon and rectum with permanent ileostomy, ileorectal anastomosis, ileal pouch-anal anastomosis, subtotal colectomy plus rectal polyposis electrocautery and anastomosis of the caecum and anus preserving the ileocecal valve [56,57,62]. However, no significant prevalence differences have been observed among these methods, because surgical outcomes depend on the skill of the surgeon and the appropriateness of the surgical method rather than personal preference.

Patients with FAP also develop adenomatous polyps in the upper gastrointestinal tract. Duodenal and ampullary polyps pose obstacles for treatment due to surgical risks. The anti-COX2 agent celexib was recently reported to have successfully prevented development of upper gastrointestinal tract polyps in two Chinese FAP patients [63]. A male and a female, both 20 years old, both with germline APC gene mutations, each had 15-41 polyps in their duodenal tract. After administration of celexib 400 mg twice per day for 12-24 months, the numbers of duodenal polyps decreased to 0-3. After electrocautery removal of the remaining polyps, both patients are free from duodenal polyps. Nonetheless, a tricky thing in these cases is the effect of anti-COX2 agent on colorectal rather than duodenal polyps, because no significant improvement has been observed in colorectal polyps in both cases. Another strategy, using sulindac to prevent the development of polyps, was used in 18 Chinese FAP cases [64]. Although both a reduction of numbers and an improvement of histopathology are observed in colorectal polyps after 12 months of administration, the difficulty remains that usually 3-6 months after stopping the administration of the drug polyps recur. A similar result was reported in Western countries. The chemopreventive effects of both NSAID and anti-COX2 agents on FAP still need further study.

Hamartomatous polyposis syndromes

Hamatomatous polyposis in the gastrointestinal tract mainly includes juvenile polyposis and Peutz-Jeghers syndrome (PJS). Few reports can be found on Chinese juvenile polyposis, but Peutz-Jeghers syndrome does not seem to be very rare in the Chinese population. A clinical analysis for 165 typical Chinese Peutz-Jeghers cases, which were collected over the past 10 years, was reported last year [65]. It was found that hamartomatous polyps of the gastrointestinal tract and freckling of the lips and buccal mucosa were the two main features of Chinese PJS. Abdominal pain and gastrointestinal bleeding were the main presentations and 58.7% of patients with abdominal pain suffered from acute intestinal obstructions. Hamartomatous polyposis is associated with a significantly increased cancer risk. In this report, 33 patients (20%) developed cancer, including 14 cases of colorectal cancer, 5 of gastric cancer and 3 of small bowel and cervix cancer. Cancers often developed at an early age and tended to be of low differentiation.

Conclusion

More and more papers on Chinese hereditary colorectal cancer are being published. Genetic patterns, clinical manifestations and management of Chinese hereditary colorectal cancer have been studied. HNPCC in the Chinese population, using national criteria for suspected HNPCC, appears to have a similar genetic background when compared with HNPCC in Western countries. However, a different tumour spectrum has been observed. Gastric cancer instead of endometrial cancer is the second most common cancer in Chinese HNPCC. Although rectal cancer is the major manifestation of sporadic colorectal cancer in China, no such preference has been observed in Chinese HNPCC patients. This suggests differences in gene-environment interaction between the two groups, which need to be further explored. The genetic background of Chinese familial adenomatous polyposis is less clear, but the management and preventative strategies of FAP are more accessible. Insight into the genetic and clinical features of both types of hereditary colorectal cancer in the Chinese population will help to prevent and manage these disorders.